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Fordyce Spots
Wikipedia
External links [ edit ] DermAtlas: Fordyce spots Fordyce spots v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease
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Stafne Defect
Wikipedia
BC Klazomenaean Hoplite Warrior”, Book of Abstracts, 37th Annual Meeting of the American Paleopathology Association, Albuquerque, New Mexico, April 13–14, 2010 v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease
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Dyssynergia
Wikipedia
Types of dyssynergia include Ramsay Hunt syndrome type 1 , bladder sphincter dyssynergia , and anal sphincter dyssynergia . ... Contents 1 Types 1.1 Ramsay Hunt syndrome type 1 1.2 Bladder sphincter dyssynergia 1.3 Anal sphincter dyssynergia 2 Diagnosis 2.1 Anal sphincter dyssynergia 2.1.1 Anorectal manometry 2.1.2 Defecography studies 2.1.3 Digital rectal examinations 3 Treatment 3.1 Bladder sphincter dyssynergia 3.1.1 Medication 3.1.2 Catheterization 3.1.3 Botox 3.1.4 Urethral stents 3.1.5 Sphincterotomy 4 See also 5 References Types [ edit ] Ramsay Hunt syndrome type 1 [ edit ] Ramsay Hunt syndrome type 1 is a rare, neurodegenerative disorder characterized by myoclonus , intention tremor , progressive ataxia and occasionally dementia . [2] [3] Bladder sphincter dyssynergia [ edit ] Bladder sphincter dyssynergia also known as detrusor sphincter dyssynergia is the decrease of detrusor (wall muscle of the bladder) pressure which causes unwanted urination. ... A catheter is then used to help relieve pressure that can occur. [10] [11] See also [ edit ] Synergy References [ edit ] ^ "Dyssynergia -- Medical Definition" . ^ "Ramsay Hunt Syndrome" . Archived from the original on 2011-08-28 . ... PMID 12494314 . v t e Symptoms and signs relating to movement and gait Gait Gait abnormality CNS Scissor gait Cerebellar ataxia Festinating gait Marche à petit pas Propulsive gait Stomping gait Spastic gait Magnetic gait Truncal ataxia Muscular Myopathic gait Trendelenburg gait Pigeon gait Steppage gait Antalgic gait Coordination Ataxia Cerebellar ataxia Dysmetria Dysdiadochokinesia Pronator drift Dyssynergia Sensory ataxia Asterixis Abnormal movement Athetosis Tremor Fasciculation Fibrillation Posturing Abnormal posturing Opisthotonus Spasm Trismus Cramp Tetany Myokymia Joint locking Paralysis Flaccid paralysis Spastic paraplegia Spastic diplegia Spastic paraplegia Syndromes Monoplegia Diplegia / Paraplegia Hemiplegia Triplegia Tetraplegia / Quadruplegia General causes Upper motor neuron lesion Lower motor neuron lesion Weakness Hemiparesis Other Rachitic rosary Hyperreflexia Clasp-knife responseCACNA2D2, CACNA1A, NPC1, SCN8A, ABCB7, SLC2A1, UROC1, GABRA1, HCN1, PIBF1, TUBB4A, CP, CACNB4, SOX2, PUM1, EGR3, ATP7A, ARCN1, ADPRS, GABRA4, YME1L1, PITRM1, RARS1, AP2M1, HK1, TWNK, SETX, POLG, ATXN3, ATM, PRNP, APTX, ITPR1, TTPA, TBP, ATP1A3, SPTBN2, ATP6, COQ8A, KCNA1, SIL1, PNKP, PNPLA6, SPG7, CA8, CSTB, COX8A, COX20, KCNA2, AARS2, GOSR2, PMM2, PEX10, SCN1A, DNAJC19, C9orf72, OPA1, MECP2, ATP2B3, PSEN1, TDP1, TTR, KCNJ10, SLC1A3, DLD, PLEKHG4, CNTNAP2, ATN1, SAMD9L, NKX2-1, EBF3, AIFM1, RUBCN, GALT, ITM2B, PRF1, ERCC4, GFAP, GJB1, GLB1, SLC52A2, DNM1L, SNX14, VPS13D, TSFM, PIK3CA, TRNE, TINF2, ND4, MVK, COX2, PIK3R5, ATP13A2, LMNB1, TDP2, ARSG, WWOX, ATP8A2, CHP1, APOB, ANK1, DARS2, SPG11, GSN, POLR3B, OPA3, AARS1, PLA2G6, STXBP1, UBE3A, TPP1, TRPC3, CLN5, PRRT2, DAB1, VAMP1, TRAK1, CEP164, SUCLG1, USH2A, DHX30, SLC6A19, RPIA, MAST1, UBAC2, FASTKD2, CNKSR2, CLRN1, KLLN, PET100, NEXMIF, TREX1, VHL, POLR3A, TUBB2B, SDCCAG8, NPC2, SLC35A1, NDUFS7, CIB2, SEC23B, VLDLR, ZNF423, MAPK8IP3, KIF1B, SPART, TCF20, TCN2, TERC, NSMF, NECAP1, PARS2, NDUFAF3, TERT, WHRN, TGFB1, COG4, FLRT3, TK2, SPIDR, ZFYVE26, ETHE1, ABCA5, TLR4, MED13L, SYNE1, SZT2, RPGRIP1L, IL12A-AS1, DMXL2, KIAA0556, VPS13A, MLC1, PMPCA, TOMM40, SLC30A9, WFS1, KIF7, BMP15, IQCB1, KLRC4, ZNF592, SDHAF1, POLR1C, MPDU1, PIGL, OFD1, PEX16, HS6ST1, CHCHD10, SNAP29, ALG11, PEX3, SLC6A5, NHLRC1, CTDP1, ELP1, NOL3, SGPL1, DCHS1, ST3GAL5, SYNJ1, SYNGAP1, CTSF, FGF17, HESX1, DPM1, CISD2, SUCLA2, FEZF1, AP3B2, PEX11B, ZNF142, SNORD118, NSD2, SEMA3A, MICU1, NELFA, ABCA7, GPHN, LRPPRC, RAD50, XPA, XPC, YWHAE, YWHAG, USH1C, SCO2, CEP104, AP5Z1, TUBA1A, TELO2, AGRN, KIAA0753, ALDH5A1, KIAA0586, FRMPD4, EPM2A, NUP214, PDHX, TCTN3, IFT140, AAAS, ABHD12, CEP120, TRAF3IP1, CEP290, TCTN2, UBA5, DHDDS, PDZD7, STN1, PANK2, CTC1, HYLS1, SRD5A3, ARMC9, NUBPL, DNAJC5, SLC19A3, COL18A1, SPRY4, C19orf12, CSPP1, ROGDI, CEP78, SLC13A3, SLC5A7, PROK2, RNASEH1, TRAPPC11, CDH23, HEPACAM, ARV1, ACD, FAT4, TMEM237, PCDH15, CPLANE1, NDUFAF5, CCDC28B, TMEM231, TCTN1, ADGRV1, TMEM107, PTPN22, MICOS13, SLC52A3, NUS1, ARL13B, RNF168, TRAPPC6B, USH1G, WDR81, NDUFA11, STX1B, SYT2, NAXE, PROKR2, TANGO2, NAGS, NDUFAF6, BEAN1, SLC46A1, TUBB, COA8, PIGY, COG8, NKX6-2, KISS1R, PIGO, ATAD1, WDR73, COX14, LYRM7, CEP41, TMEM67, C12orf65, ATPAF2, RFT1, NDUFAF2, PGAP3, PIGS, WDR19, CC2D2A, HACE1, TMEM216, TPRKB, SEPSECS, ABHD5, MECR, NDUFAF1, TACO1, GLRX5, TIMMDC1, ALG6, ACTL6B, TMEM138, PIGT, TBCE, CCDC141, OTUD6B, PTRH2, RRM2B, GMPPA, PCDH19, UQCRQ, SACS, SLC17A5, BSCL2, CYFIP2, TPK1, NPHP3, B9D1, INVS, GMPPB, COQ2, PGAP2, IL23R, FLVCR1, NDUFAF4, SUMF1, PSMC3IP, SUFU, RTEL1, ERAP1, TMEM126B, PIGV, PEX26, FRMD4A, WDR11, NAXD, MBD5, LMBRD1, INPP5E, INPP5K, NPHP4, MRPS22, PRDM8, MFSD8, NUP107, GJC2, MCOLN1, CHD7, SLC39A4, FOXRED1, ATAD3A, ADA2, RIPK4, NANS, TREM2, RNF216, NDUFB11, IL17RD, AHI1, SLC25A42, PIGG, MKS1, SLC13A5, TMEM70, CLN6, PIGW, FAM149B1, VRK1, TBCD, TRNK, COL13A1, MTTP, RNR1, TRNF, TRNH, TRNI, CCR1, ND6, TRNL1, TRNN, TRNP, TRNQ, TRNS1, TRNS2, COX6B1, ND5, KIT, ATP8, LETM1, TAT, LY6E, MEFV, COX15, MPV17, COX1, ND4L, COX3, CYTB, ND1, COX10, ND2, ND3, TRNW, MYD88, CLTC, NONO, NDUFS6, NDUFS8, ERCC3, NDUFV2, NEU1, NF2, PNP, ERCC8, NPHP1, NTRK2, OGDH, OTC, PAFAH1B1, PARN, NDUFS4, NDUFV1, NDUFS3, CHAT, NDUFS2, NDUFS1, NDUFB10, NDUFB9, NDUFB8, NDUFB3, NDUFA6, NDUFA1, CHD2, LYST, MYO9A, MYO7A, MYO5A, CPS1, KCNJ11, PCNA, GBA, GABRB3, EDNRB, GABRD, DYRK1A, GABRG2, GAMT, DUSP6, GABRB2, GBE1, GCK, GJA1, GCLC, DNMT1, GLRA1, EEF1A2, GABRB1, KCNB1, FOXI1, ERCC2, ERCC6, BPTF, FGF8, FGF12, FGFR1, EPRS1, EPB42, FMR1, FXN, CLN8, FSHR, FTL, NR5A1, GLRB, DNASE1L3, DNM1, CTSD, DCX, HMGCL, HNRNPH2, DCC, DBT, CYP27A1, CTNNA2, SARDH, IL10, IL12A, INS, PDX1, ANOS1, CSF1R, HLCS, HLA-DQB1, HLA-DQA1, HLA-B, HIC1, HEXB, DDB2, HARS1, GSS, DGUOK, DHFR, GRIN2D, GRIN2B, DKC1, GRN, DLAT, GPI, PAX6, CDC42, ERCC5, KIF1A, ARSA, RORA, ASL, ASS1, ATP1A2, SMPD1, PEX5, ATP6V1A, PEX2, PEX19, PTS, SNAI2, PTEN, AUH, PSEN2, APC, HTRA1, SNAP25, PRPS1, SORL1, BCKDHA, SOX10, SMARCB1, SARS1, PPT1, SCN3A, SDHD, SLC1A2, FAS, SLC4A1, SDHC, SDHB, SDHA, SCO1, SLC6A1, SCN9A, SCN2A, ARL3, SCN1B, ATXN8OS, SLC6A8, ATXN2, SLC12A3, SLC16A2, SLC18A3, SLC25A1, AKT1, ATXN1, SPAST, BBS1, PPP3CA, SLC26A4, C4A, PEX13, PEX12, PEX7, PEX6, PEX1, BCKDHB, ACAT1, ACADM, BTD, CACNA1B, PDGFB, SUOX, ABCC8, PDE6D, SURF1, SYT1, TACR3, PEX14, APP, PGM3, PLP1, BCS1L, SPR, STAT4, PGK1, STAT3, ACO2, SPTB, PHYH, SPTA1, ATXN7, AFP, ZFYVE9, SAR1A, AFG3L2, STUB1, TPO, GRM1, PDYN, CAPN1, PPP2R2B, CASP3, TGM6, EIF2B1, MRE11, FGF14, SLC9A6, CBLL2, PRND, HSD17B4, PRKCG, PRKN, MSTO1, MUL1, ATCAY, KCNC1, IREB2, GRID2, EIF2S2, EIF2B2, SLC9A1, EIF2B4, HTT, DOCK3, CERNA3, ACHE, GBA2, SOD1, ANO10, XRCC1, TP53, KCNC3, ATXN10, MAPK1, AR, PDHA1, RELN, SQSTM1, NUP93, CAMTA1, RFC1, PCYT1A, PRICKLE1, CTBP1, SAMD9, IGFALS, TSHZ1, USP14, C20orf181, BRCA1, ENO2, ACR, CDKN1A, CDC25C, BDNF, MINDY3, CDK1, MEF2B, CCND1, MIR3191, KRIT1, SCA37, CBLN1, CBLN4, HT, ERBB2, TTBK2, FMR1-IT1, CALM3, CALM2, BCL6, ALK, ATXN7L3B, CRK, ARSH, LMNB2, DAP, ABCD1, SLC25A46, TIMM8A, ALAS2, MAPK14, COA6, CRMP1, CHD6, CALM1, MARS2, ACTB, CRH, SCA18, ARMH1, SLC9C2, ADGRB3, NLRP3, SCA26, PARP1, FBXO32, XRCC6P5, CHRNA4, ZUP1, PRUNE2, LIG3, CAMKMT, PIK3CG, ARHGEF2, RNASE2, RFX3, PPT2, GRAP2, ATG5, PSMD7, KIF20B, RGS6, PKN1, MTSS1, POLD1, PLS3, PIK3CD, CILK1, PIK3CB, RABEPK, LANCL1, WARS2, NOP56, AHSA1, KHDRBS1, CPLX1, UTS2, EBNA1BP2, SLC7A9, CHEK2, PAH, RPS4X, S100B, TRPA1, HSPB3, SYP, TGM2, ELOVL4, TOP1, TOP2A, TPM3, TRH, TRIO, TRPC1, SPTBN1, TUBB2A, UCHL1, UCN, UTRN, ABCA2, SOX4, ZIC1, ZIC2, AIMP2, CCDC6, SLC6A3, CUL4B, SGCG, SEL1L, DENR, TP63, CACNA1G, MGLL, OPHN1, FGF9, GOLGA2, IFNG, HSPD1, HSPB2, HSPB1, HSPA4, HMBS, CWF19L1, UEVLD, CXCL2, GRM5, NLRP2, GRIN2A, GRB2, GNAL, OGG1, GLUD2, SLC12A9, GH1, TBC1D24, NUFIP2, KLHL1, TP53INP2, GAA, ANO3, FUS, PINK1, FRAXA, FOXO3, PANK1, IFRD1, MAP3K20, IL9, NTRK1, FAN1, NPY, NFASC, NCDN, MTCL1, BRD4, NBN, DAPK2, SUN2, GCA, MTO1, RNF19A, POLDIP2, FGF21, SEZ6L2, ANKRD1, MID1, SMAD2, RPSA, KIF5B, KCNN3, KCNMA1, KCNC2, RNF138, KCNA6, KCNA5, H3P28
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Propionic Acidemia
Wikipedia
Classification D ICD - 10 : E71.1 ICD - 10-CM : E71.121 ICD - 9-CM : 270.3 OMIM : 606054 MeSH : D056693 DiseasesDB : 29673 External resources eMedicine : ped/1906 Orphanet : 35 v t e Inborn error of amino acid metabolism K → acetyl-CoA Lysine /straight chain Glutaric acidemia type 1 type 2 Hyperlysinemia Pipecolic acidemia Saccharopinuria Leucine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency 3-Methylglutaconic aciduria 1 Isovaleric acidemia Maple syrup urine disease Tryptophan Hypertryptophanemia G G→ pyruvate → citrate Glycine D-Glyceric acidemia Glutathione synthetase deficiency Sarcosinemia Glycine → Creatine : GAMT deficiency Glycine encephalopathy G→ glutamate → α-ketoglutarate Histidine Carnosinemia Histidinemia Urocanic aciduria Proline Hyperprolinemia Prolidase deficiency Glutamate / glutamine SSADHD G→ propionyl-CoA → succinyl-CoA Valine Hypervalinemia Isobutyryl-CoA dehydrogenase deficiency Maple syrup urine disease Isoleucine 2-Methylbutyryl-CoA dehydrogenase deficiency Beta-ketothiolase deficiency Maple syrup urine disease Methionine Cystathioninuria Homocystinuria Hypermethioninemia General BC / OA Methylmalonic acidemia Methylmalonyl-CoA mutase deficiency Propionic acidemia G→ fumarate Phenylalanine / tyrosine Phenylketonuria 6-Pyruvoyltetrahydropterin synthase deficiency Tetrahydrobiopterin deficiency Tyrosinemia Alkaptonuria / Ochronosis Tyrosinemia type I Tyrosinemia type II Tyrosinemia type III / Hawkinsinuria Tyrosine → Melanin Albinism : Ocular albinism ( 1 ) Oculocutaneous albinism ( Hermansky–Pudlak syndrome ) Waardenburg syndrome Tyrosine → Norepinephrine Dopamine beta hydroxylase deficiency reverse: Brunner syndrome G→ oxaloacetate Urea cycle / Hyperammonemia ( arginine aspartate ) Argininemia Argininosuccinic aciduria Carbamoyl phosphate synthetase I deficiency Citrullinemia N-Acetylglutamate synthase deficiency Ornithine transcarbamylase deficiency / translocase deficiency Transport / IE of RTT Solute carrier family : Cystinuria Hartnup disease Iminoglycinuria Lysinuric protein intolerance Fanconi syndrome : Oculocerebrorenal syndrome Cystinosis Other 2-Hydroxyglutaric aciduria Aminoacylase 1 deficiency Ethylmalonic encephalopathy Fumarase deficiency Trimethylaminuria v t e Inborn error of lipid metabolism : fatty-acid metabolism disorders Synthesis Biotinidase deficiency (BTD) Degradation Acyl transport Carnitine CPT1 CPT2 CDSP CACTD Adrenoleukodystrophy (ALD) Beta oxidation General Acyl CoA dehydrogenase Short-chain SCADD Medium-chain MCADD Long-chain 3-hydroxy LCHAD Very long-chain VLCADD Mitochondrial trifunctional protein deficiency (MTPD): Acute fatty liver of pregnancy Unsaturated 2,4 Dienoyl-CoA reductase deficiency (DECRD) Odd chain Propionic acidemia (PCC deficiency) Other 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (HADHD) Glutaric acidemia type 2 (MADD) To acetyl-CoA Malonic aciduria (MCD) Aldehyde Sjögren–Larsson syndrome (SLS)
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Trigger Finger
Wikipedia
Not to be confused with De Quervain syndrome . Trigger finger Other names Historicopous, trigger digit, trigger thumb, [1] stenosing tenosynovitis [1] Play media An example of trigger finger affecting the ring finger Specialty Plastic surgery Symptoms Catching or locking of the involved finger, pain [2] [3] Usual onset 50s to 60s years old [2] Risk factors Repeated injury, diabetes , kidney disease, thyroid disease, inflammatory disease [3] Diagnostic method Based on symptoms [2] Differential diagnosis Fracture, tumor, injury [2] Treatment Rest, splinting the finger, NSAIDs , steroid injections, surgery [3] Frequency Relatively common [2] Trigger finger , also known as stenosing tenosynovitis , is a disorder characterized by catching or locking of the involved finger. [2] Pain may occur in the palm of the hand or knuckles. [3] The name is due to the popping sound made by the affected finger when moved. [2] Most commonly the ring finger or thumb is affected. [1] Risk factors include repeated injury, diabetes , kidney disease, thyroid disease, and inflammatory disease. [3] The underlying mechanism involves the tendon sheath being too narrow for the flexor tendon . [3] This typically occurs at the level of the A1 pulley . [2] While often referred to as a type of stenosing tenosynovitis , little inflammation appears to be present. [3] Diagnosis is typically based on symptoms after excluding other possible causes. [2] Initial treatment is generally with rest, splinting the finger, NSAIDs , or steroid injections. [3] If this is not effective surgery may be used. [3] Trigger finger is relatively common. [2] Females are affected more often than males. [3] Those in their 50s and 60s are most commonly affected. [2] The condition was formally described in 1850. [2] Contents 1 Signs and symptoms 2 Causes 3 Diagnosis 4 Treatment 4.1 Surgery 5 Prognosis 6 References 7 External links Signs and symptoms [ edit ] Symptoms include catching or locking of the involved finger. [2] As the disease progresses pain may occur in the palm of the hand or knuckles. [3] In the ring and middle fingers, often a nodule can be felt at the area of the hand where the palm meets the finger. [4] Causes [ edit ] The cause of trigger finger is unclear but several causes have been proposed. [2] It has also been called stenosing tenosynovitis (specifically digital tenosynovitis stenosans ), but this may be a misnomer, as inflammation is not a predominant feature. ... While the mechanism is unclear, there is some evidence that triggering of the thumb is more likely to occur following surgery for carpal tunnel syndrome . [7] It may also occur in rheumatoid arthritis . ... Video of Trigger Finger Release Surgery on YouTube American Academy of Orthopaedic Surgeons information on trigger finger Information from the Mayo Clinic v t e Soft tissue disorders Capsular joint Synoviopathy Synovitis / Tenosynovitis Calcific tendinitis Stenosing tenosynovitis Trigger finger De Quervain syndrome Transient synovitis Ganglion cyst osteochondromatosis Synovial osteochondromatosis Plica syndrome villonodular synovitis Giant-cell tumor of the tendon sheath Bursopathy Bursitis Olecranon Prepatellar Trochanteric Subacromial Achilles Retrocalcaneal Ischial Iliopsoas Synovial cyst Baker's cyst Calcific bursitis Noncapsular joint Symptoms Ligamentous laxity Hypermobility Enthesopathy / Enthesitis / Tendinopathy upper limb Adhesive capsulitis of shoulder Impingement syndrome Rotator cuff tear Golfer's elbow Tennis elbow lower limb Iliotibial band syndrome Patellar tendinitis Achilles tendinitis Calcaneal spur Metatarsalgia Bone spur other/general: Tendinitis / Tendinosis Nonjoint Fasciopathy Fasciitis : Plantar Nodular Necrotizing Eosinophilic Fibromatosis / contracture Dupuytren's contracture Plantar fibromatosis Aggressive fibromatosis Knuckle pads
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Oral Mucocele
Wikipedia
External links [ edit ] Classification D ICD - 10 : K11.6 ICD - 9-CM : 527.6 , 528.9 MeSH : D009078 DiseasesDB : 30713 External resources eMedicine : derm/274 v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease
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Genital Ulcer
Wikipedia
The most common causes of a genital ulcer include infectious agents, with sexually transmitted diseases being the most common, but which can also include fungal infections and secondary bacterial infections. [2] While infectious agents are the most common cause, a genital ulcer may also be the result of non-infectious causes such as Behcet's syndrome , lupus , or psoriasis . [4] Since it is difficult to determine a cause of a genital ulcer from history, examination, and population characteristics alone, further testing is often needed. ... The most common non-infectious sources of genital ulcers are first Behcet's disease, and second drug reaction. [2] Behcet's syndrome is a chronic systemic vasculitis infection that is defined by recurrent oral and genital aphthous ulcers but can also affect many other organ systems, such as the eyes, ears, nervous system, heart, lungs, joints, and intestines. [10] Behcet's syndrome commonly presents in the 30-40 age range [10] and is more common in the Middle East and Asia. [11] There is a familial component to Behcet's syndrome since it has associations with the HLA-B51 gene. [10] Causes of drug induced genital ulcers take the form of Stevens–Johnson syndrome , toxic epidermal necrolysis , erythema multiforme , and fixed drug eruptions in response to a diverse list of medications. [10] Stevens–Johnson syndrome and toxic epidermal necrolysis are more likely than erythema multiforme to have genital manifestations although all present with a toxic appearing patient. [10] A fixed drug eruption in comparison does not present as a toxic appearing patient but rather single or multiple erythematous patches that vary in size and shape which eventually turn dark brown in color and become itchy. [10] The defining characteristic is that these drug eruptions appear in the same location each time the offending medication is used, and will resolve on their own. [10] Other potential causes of non-infectious genital ulcers are diverse, but can include sexual trauma, Lipschutz ulcers , inflammatory bowel diseases such as Crohn's disease, lichen planus, lichen sclerosis, and immunobullous disease such as pemphigous vulgaris, since bullous pemphigoid is less likely to occur on the genitals. [10] Cancers of the vulva and penis, with the most common subtype being squamous cell carcinoma, can also present as genital ulcers, but leukemias such as chronic lymphocytic leukemia and acute promyelotic leukemia have also been identified. [10] Infectious non-sexually transmitted causes [ edit ] Even lesser common etiologies of genital ulcers include fungal infection, secondary bacterial infections, and parasitic infections. [10] [4] Fungal infections are rare causes of genital ulcers, but candida albicans infection is typically the most common source, and is more prevalent in patients with a history of diabetes mellitus, chronic steroid use, or other immunodeficiencies. [10] There have also been rare case reports of paracoccidioidomycosis, zygomycosis and histoplasmosis infections causing genital ulcers. [10] Parasitic infections such as amoebiasis and leishmaniasis can present in cutaneous form in the genital regions.
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Leiomyoma
Wikipedia
Polycythemia may occur due to increased erythropoietin production as part of a paraneoplastic syndrome . The word is from leio- + myo- + -oma , "smooth-muscle tumor". ... External links [ edit ] Classification D ICD - 10 : D21 , D25 ( ILDS D21.M40) ICD - 9-CM : 218 ICD-O : M8890/0 -8894 MeSH : D007889 External resources MedlinePlus : dostinex Esophageal Leiomyoma at eMedicine v t e Diseases of the skin and appendages by morphology Growths Epidermal Wart Callus Seborrheic keratosis Acrochordon Molluscum contagiosum Actinic keratosis Squamous-cell carcinoma Basal-cell carcinoma Merkel-cell carcinoma Nevus sebaceous Trichoepithelioma Pigmented Freckles Lentigo Melasma Nevus Melanoma Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma (benign fibrous histiocytoma) Keloid Lipoma Neurofibroma Xanthoma Kaposi's sarcoma Infantile digital fibromatosis Granular cell tumor Leiomyoma Lymphangioma circumscriptum Myxoid cyst Rashes With epidermal involvement Eczematous Contact dermatitis Atopic dermatitis Seborrheic dermatitis Stasis dermatitis Lichen simplex chronicus Darier's disease Glucagonoma syndrome Langerhans cell histiocytosis Lichen sclerosus Pemphigus foliaceus Wiskott–Aldrich syndrome Zinc deficiency Scaling Psoriasis Tinea ( Corporis Cruris Pedis Manuum Faciei ) Pityriasis rosea Secondary syphilis Mycosis fungoides Systemic lupus erythematosus Pityriasis rubra pilaris Parapsoriasis Ichthyosis Blistering Herpes simplex Herpes zoster Varicella Bullous impetigo Acute contact dermatitis Pemphigus vulgaris Bullous pemphigoid Dermatitis herpetiformis Porphyria cutanea tarda Epidermolysis bullosa simplex Papular Scabies Insect bite reactions Lichen planus Miliaria Keratosis pilaris Lichen spinulosus Transient acantholytic dermatosis Lichen nitidus Pityriasis lichenoides et varioliformis acuta Pustular Acne vulgaris Acne rosacea Folliculitis Impetigo Candidiasis Gonococcemia Dermatophyte Coccidioidomycosis Subcorneal pustular dermatosis Hypopigmented Tinea versicolor Vitiligo Pityriasis alba Postinflammatory hyperpigmentation Tuberous sclerosis Idiopathic guttate hypomelanosis Leprosy Hypopigmented mycosis fungoides Without epidermal involvement Red Blanchable Erythema Generalized Drug eruptions Viral exanthems Toxic erythema Systemic lupus erythematosus Localized Cellulitis Abscess Boil Erythema nodosum Carcinoid syndrome Fixed drug eruption Specialized Urticaria Erythema ( Multiforme Migrans Gyratum repens Annulare centrifugum Ab igne ) Nonblanchable Purpura Macular Thrombocytopenic purpura Actinic/solar purpura Papular Disseminated intravascular coagulation Vasculitis Indurated Scleroderma / morphea Granuloma annulare Lichen sclerosis et atrophicus Necrobiosis lipoidica Miscellaneous disorders Ulcers Hair Telogen effluvium Androgenic alopecia Alopecia areata Systemic lupus erythematosus Tinea capitis Loose anagen syndrome Lichen planopilaris Folliculitis decalvans Acne keloidalis nuchae Nail Onychomycosis Psoriasis Paronychia Ingrown nail Mucous membrane Aphthous stomatitis Oral candidiasis Lichen planus Leukoplakia Pemphigus vulgaris Mucous membrane pemphigoid Cicatricial pemphigoid Herpesvirus Coxsackievirus Syphilis Systemic histoplasmosis Squamous-cell carcinoma v t e Connective / soft tissue tumors and sarcomas Not otherwise specified Soft-tissue sarcoma Desmoplastic small-round-cell tumor Connective tissue neoplasm Fibromatous Fibroma / fibrosarcoma : Dermatofibrosarcoma protuberans Desmoplastic fibroma Fibroma / fibromatosis : Aggressive infantile fibromatosis Aponeurotic fibroma Collagenous fibroma Diffuse infantile fibromatosis Familial myxovascular fibromas Fibroma of tendon sheath Fibromatosis colli Infantile digital fibromatosis Juvenile hyaline fibromatosis Plantar fibromatosis Pleomorphic fibroma Oral submucous fibrosis Histiocytoma / histiocytic sarcoma : Benign fibrous histiocytoma Malignant fibrous histiocytoma Atypical fibroxanthoma Solitary fibrous tumor Myxomatous Myxoma / myxosarcoma Cutaneous myxoma Superficial acral fibromyxoma Angiomyxoma Ossifying fibromyxoid tumour Fibroepithelial Brenner tumour Fibroadenoma Phyllodes tumor Synovial -like Synovial sarcoma Clear-cell sarcoma Lipomatous Lipoma / liposarcoma Myelolipoma Myxoid liposarcoma PEComa Angiomyolipoma Chondroid lipoma Intradermal spindle cell lipoma Pleomorphic lipoma Lipoblastomatosis Spindle cell lipoma Hibernoma Myomatous general: Myoma / myosarcoma smooth muscle : Leiomyoma / leiomyosarcoma skeletal muscle : Rhabdomyoma / rhabdomyosarcoma : Embryonal rhabdomyosarcoma Sarcoma botryoides Alveolar rhabdomyosarcoma Leiomyoma Angioleiomyoma Angiolipoleiomyoma Genital leiomyoma Leiomyosarcoma Multiple cutaneous and uterine leiomyomatosis syndrome Multiple cutaneous leiomyoma Neural fibrolipoma Solitary cutaneous leiomyoma STUMP Complex mixed and stromal Adenomyoma Pleomorphic adenoma Mixed Müllerian tumor Mesoblastic nephroma Wilms' tumor Malignant rhabdoid tumour Clear-cell sarcoma of the kidney Hepatoblastoma Pancreatoblastoma Carcinosarcoma Mesothelial Mesothelioma Adenomatoid tumorESR1, SMAD3, TSC2, SFRP1, WNT5B, INHBA, BCL2, PCNA, PARP1, BAX, EZH2, MKI67, TGFBR1, MYC, HMGA2, PGR, IGF1, IGF2, TP53, CYP19A1, TGFB3, FH, MED12, KIT, FN1, CTNNB1, CDKN2A, VCAN, TGFB1, COMT, AR, FGF2, VEGFA, CYP17A1, ACTB, ESR2, EGF, DES, MMRN1, MMP2, KAT6B, EDN1, CD6, GPER1, CXCL8, CYP1A1, MDM2, CCN1, CYP2B6, GSTM1, DNMT1, EGFR, EGR1, PLAG1, CUX1, TNF, MIR29C, MIR21, MIR200C, KANSL1, ALK, CCND1, PRL, COL1A1, PTEN, CD24, GAPDH, GJA1, PRLHR, PBX3, IGFBP2, PTCH1, FMOD, MUC16, HOXA10, HTC2, CD274, IGF1R, PTGS2, SPIN1, SMAD7, MCL1, SMAD4, RBP1, SMAD2, SHBG, KRAS, TERT, TXN, DLEC1, IL4, YWHAG, IL2, PAEP, IGFBP3, SQSTM1, SERPINE1, H3P10, CD34, ACE, EPO, ALDH1A1, DPT, CDH1, DNMT3A, EWSR1, CCN2, EDNRB, CASP3, CYP1B1, CAV1, SLC27A4, DEPDC5, HDAC6, AKT3, ARNT, MVP, ATF3, NCOR2, ABI2, NCOR1, SLC7A8, ADAMTS4, CHST3, TSIX, EBI3, TNRC6B, RFTN1, SDS, ANGPT2, FST, NCOA2, ATG7, PPIG, KHDRBS1, EBP, NFAT5, NES, WASF3, APEX1, FERMT2, AKAP13, SPINT2, ARTN, KLF4, CA2, XRCC1, XPC, XIST, WNT7A, LAT2, VWF, DST, CALD1, XRCC4, TSC1, TP53BP1, SEC62, TIMP2, TIE1, THBS2, THBS1, XRCC3, BMP2, PTTG1, BECN1, SMUG1, SNURF, BAK1, CCN5, IL18R1, TNFSF9, TNFSF10, NCOA1, NR4A3, TP63, IFITM1, KLF11, RECK, TKTL1, SLC7A5, BCL6, ANGPT1, FGFR3, NUP62, SLC27A1, MIR15B, MIR150, MIRLET7C, MIRLET7A1, SERTM2, CASC15, TBPL2, GADL1, TES, HCAR2, AHR, TET3, PLD5, FAM9A, ADAMTS15, DNAJB7, MIR182, MIR197, AGTR2, AGRP, LOC110806263, MTCO2P12, PGR-AS1, RNA5SP202, TRG-GCC5-1, ACTG1, POTEF, POU5F1P4, POU5F1P3, POTEM, MIR146B, MIR93, PLIN2, MIR29A, MIR221, MAGEC3, OSCP1, RXFP2, ADCY10, ATF7IP, MEG3, ANO1, ANGPT4, BET1L, DCTN4, AKR1B1, SLC27A6, PCDH11X, HPGDS, PDCD4, AGO2, FOXP1, SNORD56, CCND2, EDEM2, HDAC8, CYCSP25, RXFP1, GNRHR2, AZIN2, MED8, NACC1, AKT2, LINC00473, ATAD1, NLRC5, ADGRV1, FERMT3, PDCD1LG2, TET1, NANOG, SNIP1, GGCT, PTPN22, TACR3, CCNG1, ATN1, ITGA2, INSR, DRD1, IL18, CXCR1, DRD2, IL6, EDNRA, TFAP2C, IL1RN, IL1B, IKBKB, IGFBP7, EFNA4, EGR2, IGFBP1, ITGAV, ITGB1, KRT19, LAMB1, MME, DAPK1, MEST, MEN1, DBI, MAP2, DFFA, DFFB, DHCR24, SARDH, LTBP2, LTBP1, CYP4F3, LGALS3, LEP, EPHB2, ERBB2, IFNA13, GRB2, GNRHR, GNRH2, GNRH1, GLI1, FBLN1, GHR, GH1, MSTN, FBN1, FZD2, MTOR, EFEMP1, FGF1, FOXO3, FGFR1, F3, GRIA2, IFNA1, NR3C1, IFI27, TNC, ERBB3, HSPA1B, HSPA1A, HSD17B2, HRAS, HPGD, HOXA11, ERCC2, HMGN2, HIF1A, GTF2H1, ETS1, GRM2, MMP1, MPO, MSH2, SLC5A3, SLC3A2, SLC2A4, SLC2A1, SHH, SFRP4, CDK2, SDHB, CCL2, SATB1, SALL1, S100A11, S100A4, RXRA, TRIM27, REST, SMTN, SMARCB1, PLAAT4, SMN1, CD44, TEK, FGR, TACR1, TAC3, TACR2, TAC1, SYP, STK11, SRC, SPINT1, SOX2, SORD, SNRPN, SMN2, CDKN1A, RAD51B, COX2, CPN1, PECAM1, PDGFRA, PCP4, CPN2, CR2, CSF2, PEBP1, OXTR, OGG1, NTS, NOS3, NGF, NEUROG1, MYLK, CTSL, PGAM1, PIK3CA, PTHLH, PIK3CB, CDKN1B, CEBPB, COL3A1, PSMB9, PRLR, COL4A5, MAPK1, PPP4C, PPARG, POU5F1, PLXNA2, PLP1, COL4A6, PIK3CG, PIK3CD, ACP1
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Drooling
Wikipedia
NIH site on drooling v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic diseaseTAC1, AGTR2, FRMPD4, ZBTB11, CNTNAP2, FTSJ1, AP4E1, VPS13A, SPART, IQSEC2, CNKSR2, AP4S1, IL1RAPL1, POLR3A, MID2, PDE10A, AP4B1, MTHFS, SLC9A6, IKZF1, ATP6AP2, CERT1, MED12, SRPX2, SETD5, VAC14, SLC9A7, USP27X, TUBB2B, ZNF81, ARX, PTCHD1, TANGO2, RAB39B, FOXP2, GPT2, GFM2, POLR3B, ALG13, UPF3B, IRF2BPL, CXorf56, BCORL1, ALS2, SLC12A5, KIF15, ZC4H2, ZEB2, KMT2B, ATP1A3, ACSL4, MECP2, HLA-B, HCFC1, GRIN2A, GNS, GDI1, GCH1, GABRG2, FOXG1, EIF2S3, GABBR2, DMD, DLG3, DLAT, COL2A1, CLCN4, CACNA1C, ATRX, ATP7B, ATP6V1A, MIPEP, MRE11, PAK3, PMP22, ARHGEF6, NRXN1, TRIP12, AP4M1, USP9X, ZNF41, ZNF711, UBE3A, TSPAN7, TH, TCF4, SYP, SLC16A2, SCN8A, RPS6KA3, QDPR, PTS, PTCH1, PRPS1, ST20-MTHFS
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Amalgam Tattoo
Wikipedia
External links [ edit ] Classification D v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease
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Conjugate Gaze Palsy
Wikipedia
These lesions can be caused by stroke , or conditions such as Koerber-Salus-Elschnig syndrome, Progressive supranuclear palsy , Olivopontocerebellar syndrome , Niemann-Pick Disease, Type C , or envenomation such as from a scorpion bite. [3] Mechanism [ edit ] The location of the lesion determines the type of palsy. ... This damage normally happens in the oculomotor nucleus of the midbrain [10] As in horizontal saccadic palsy, the saccades are stopped or slowed from the disrupted pathway, only in this case the signal is disrupted before it reaches the PPRF. One-and-a-half syndrome is associated with damage to the paramedian pontine reticular formation and the medial longitudinal fasciculus . [11] These combined damages cause both a complete gaze impairment on the ipsilateral side and a "half" gaze impairment on the contralateral side. [6] As seen in horizontal saccadic palsy, the impairment of the contralateral side gaze is caused by the disrupted pathways coming from the PPRF, while the "half" impairment is from the signal passing through the medial longitudinal fascicles not being able to reach its target. One-and-a-Half syndrome is normally associated with horizontal gaze. Although more rare than horizontal, one-and-a-half syndrome from damage to the paramedian pontine reticular formation and the medial longitudinal fasciculus can be shown to affect vertical gaze. ... "Coexisting vertical and horizontal one and a half syndromes" . Journal of Neurology, Neurosurgery & Psychiatry . 69 (3): 401–2. doi : 10.1136/jnnp.69.3.401 .
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Necrotizing Sialometaplasia
Wikipedia
External links [ edit ] Classification D ICD - 10 : K11.8 MeSH : D012797 DiseasesDB : 31434 External resources eMedicine : derm/656 v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth Pulp calcification Pulp stone Pulp canal obliteration Pulp necrosis Pulp polyp Pulpitis Regional odontodysplasia Resorption Shovel-shaped incisors Supernumerary root Taurodontism Trauma Avulsion Cracked tooth syndrome Vertical root fracture Occlusal Tooth loss Edentulism Tooth wear Abrasion Abfraction Acid erosion Attrition Periodontium ( gingiva , periodontal ligament , cementum , alveolus ) – Gums and tooth-supporting structures Cementicle Cementoblastoma Gigantiform Cementoma Eruption cyst Epulis Pyogenic granuloma Congenital epulis Gingival enlargement Gingival cyst of the adult Gingival cyst of the newborn Gingivitis Desquamative Granulomatous Plasma cell Hereditary gingival fibromatosis Hypercementosis Hypocementosis Linear gingival erythema Necrotizing periodontal diseases Acute necrotizing ulcerative gingivitis Pericoronitis Peri-implantitis Periodontal abscess Periodontal trauma Periodontitis Aggressive As a manifestation of systemic disease Chronic Perio-endo lesion Teething Periapical, mandibular and maxillary hard tissues – Bones of jaws Agnathia Alveolar osteitis Buccal exostosis Cherubism Idiopathic osteosclerosis Mandibular fracture Microgenia Micrognathia Intraosseous cysts Odontogenic : periapical Dentigerous Buccal bifurcation Lateral periodontal Globulomaxillary Calcifying odontogenic Glandular odontogenic Non-odontogenic: Nasopalatine duct Median mandibular Median palatal Traumatic bone Osteoma Osteomyelitis Osteonecrosis Bisphosphonate-associated Neuralgia-inducing cavitational osteonecrosis Osteoradionecrosis Osteoporotic bone marrow defect Paget's disease of bone Periapical abscess Phoenix abscess Periapical periodontitis Stafne defect Torus mandibularis Temporomandibular joints , muscles of mastication and malocclusions – Jaw joints, chewing muscles and bite abnormalities Bruxism Condylar resorption Mandibular dislocation Malocclusion Crossbite Open bite Overbite Overeruption Overjet Prognathia Retrognathia Scissor bite Maxillary hypoplasia Temporomandibular joint dysfunction Salivary glands Benign lymphoepithelial lesion Ectopic salivary gland tissue Frey's syndrome HIV salivary gland disease Necrotizing sialometaplasia Mucocele Ranula Pneumoparotitis Salivary duct stricture Salivary gland aplasia Salivary gland atresia Salivary gland diverticulum Salivary gland fistula Salivary gland hyperplasia Salivary gland hypoplasia Salivary gland neoplasms Benign: Basal cell adenoma Canalicular adenoma Ductal papilloma Monomorphic adenoma Myoepithelioma Oncocytoma Papillary cystadenoma lymphomatosum Pleomorphic adenoma Sebaceous adenoma Malignant: Acinic cell carcinoma Adenocarcinoma Adenoid cystic carcinoma Carcinoma ex pleomorphic adenoma Lymphoma Mucoepidermoid carcinoma Sclerosing polycystic adenosis Sialadenitis Parotitis Chronic sclerosing sialadenitis Sialectasis Sialocele Sialodochitis Sialosis Sialolithiasis Sjögren's syndrome Orofacial soft tissues – Soft tissues around the mouth Actinomycosis Angioedema Basal cell carcinoma Cutaneous sinus of dental origin Cystic hygroma Gnathophyma Ludwig's angina Macrostomia Melkersson–Rosenthal syndrome Microstomia Noma Oral Crohn's disease Orofacial granulomatosis Perioral dermatitis Pyostomatitis vegetans Other Eagle syndrome Hemifacial hypertrophy Facial hemiatrophy Oral manifestations of systemic disease
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Mental Retardation, Autosomal Dominant 22
Omim
., 2018). Chromosome 1q43-q44 deletion syndrome is characterized by moderate to severe mental retardation, limited or no speech, and variable but characteristic facial features, including round face, prominent forehead, flat nasal bridge, hypertelorism, epicanthal folds, and low-set ears. ... She also had hand stereotypies, intense eye communication, breathing disturbances, and screaming spells, suggesting a diagnosis of atypical Rett syndrome (RTT; 312750), but sequencing of the MECP2 (300005) gene revealed no mutations. ... The patient's features were similar to those found in patients with the chromosome 1q43-q44 deletion syndrome. In a girl with MRD22, Lopes et al. (2016) identified a de novo heterozygous nonsense mutation in the ZBTB18 gene (R186X; 608433.0002). ... The phenotype in the mutant mice resembled that seen in patients with chromosome 1q43-q44 deletion syndrome. INHERITANCE - Autosomal dominant GROWTH Height - Short stature Other - Poor growth HEAD & NECK Head - Microcephaly Face - Round face - Prominent forehead - Micrognathia - Smooth philtrum Ears - Low-set ears - Malformed ears Eyes - Hypertelorism - Epicanthal folds Nose - Flat nasal bridge Mouth - Thin upper lip NEUROLOGIC Central Nervous System - Delayed psychomotor development - Mental retardation - Poor or absent speech - Seizures - Hypotonia - Agenesis of the corpus callosum MISCELLANEOUS - Two unrelated patients with a point mutation in the ZBTB18 gene has been reported (last curated April 2017) - Variable phenotype - Incomplete penetrance of some features - Variable expressivity - Contiguous gene deletion syndrome (in most patients) MOLECULAR BASIS - Caused by mutation in the zinc finger and BTB domain containing 18 gene (ZBTB18, 608433.0001 ) - Contiguous gene deletion syndrome caused by deletion (3.5Mb) of 1q32-q44 ▲ Close
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Prolidase Deficiency
Wikipedia
External links [ edit ] Classification D ICD - 10 : E72.8 OMIM : 170100 MeSH : D056732 DiseasesDB : 29838 External resources Orphanet : 742 Prolidase deficiency on OrphaNet v t e Inborn error of amino acid metabolism K → acetyl-CoA Lysine /straight chain Glutaric acidemia type 1 type 2 Hyperlysinemia Pipecolic acidemia Saccharopinuria Leucine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency 3-Methylglutaconic aciduria 1 Isovaleric acidemia Maple syrup urine disease Tryptophan Hypertryptophanemia G G→ pyruvate → citrate Glycine D-Glyceric acidemia Glutathione synthetase deficiency Sarcosinemia Glycine → Creatine : GAMT deficiency Glycine encephalopathy G→ glutamate → α-ketoglutarate Histidine Carnosinemia Histidinemia Urocanic aciduria Proline Hyperprolinemia Prolidase deficiency Glutamate / glutamine SSADHD G→ propionyl-CoA → succinyl-CoA Valine Hypervalinemia Isobutyryl-CoA dehydrogenase deficiency Maple syrup urine disease Isoleucine 2-Methylbutyryl-CoA dehydrogenase deficiency Beta-ketothiolase deficiency Maple syrup urine disease Methionine Cystathioninuria Homocystinuria Hypermethioninemia General BC / OA Methylmalonic acidemia Methylmalonyl-CoA mutase deficiency Propionic acidemia G→ fumarate Phenylalanine / tyrosine Phenylketonuria 6-Pyruvoyltetrahydropterin synthase deficiency Tetrahydrobiopterin deficiency Tyrosinemia Alkaptonuria / Ochronosis Tyrosinemia type I Tyrosinemia type II Tyrosinemia type III / Hawkinsinuria Tyrosine → Melanin Albinism : Ocular albinism ( 1 ) Oculocutaneous albinism ( Hermansky–Pudlak syndrome ) Waardenburg syndrome Tyrosine → Norepinephrine Dopamine beta hydroxylase deficiency reverse: Brunner syndrome G→ oxaloacetate Urea cycle / Hyperammonemia ( arginine aspartate ) Argininemia Argininosuccinic aciduria Carbamoyl phosphate synthetase I deficiency Citrullinemia N-Acetylglutamate synthase deficiency Ornithine transcarbamylase deficiency / translocase deficiency Transport / IE of RTT Solute carrier family : Cystinuria Hartnup disease Iminoglycinuria Lysinuric protein intolerance Fanconi syndrome : Oculocerebrorenal syndrome Cystinosis Other 2-Hydroxyglutaric aciduria Aminoacylase 1 deficiency Ethylmalonic encephalopathy Fumarase deficiency Trimethylaminuria
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Endolymphatic Sac Tumor
Wikipedia
This tumor shows a very high association with von Hippel-Lindau syndrome (VHL). [1] Contents 1 Classification 2 Signs and symptoms 3 Imaging findings 4 Pathogenesis 5 Pathology findings 5.1 Immunohistochemistry 5.2 Cytogenetics 6 Differential Diagnosis 7 Management 8 Epidemiology 9 References 10 Further reading Classification [ edit ] The ELST has been referred to as adenocarcinoma of endolymphatic sac, Heffner tumor, [1] papillary adenomatous tumor, aggressive papillary adenoma, invasive papillary cystadenoma, and papillary tumor of temporal bone. ... Alternatively, symptom onset may be sudden, due to intralabyrinthine hemorrhage. [4] Patients may also present with other symptoms related to von Hippel-Lindau syndrome in other anatomic sites, which will result in imaging evaluation of the head. [1] [3] [5] Imaging findings [ edit ] CT in patient with VHL syndrome through the petrous ridge demonstrates bone erosion at the site of the endolymphatic sac tumor, typical of the locally aggressive behavior of this tumor (curved arrow). ... There are usually several other tumors which are part of the syndrome, including tumors of the central nervous system , kidneys , pancreas , adrenal glands , epididymis , broad ligament , along with the endolymphatic sac. The vast majority of patients with an endolymphatic sac tumor have von Hippel-Lindau syndrome. [8] [9] Pathology findings [ edit ] An intermediate power image of an endolymphatic sac tumor with bone (upper left).
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2-Hydroxyglutaric Aciduria
Wikipedia
External links [ edit ] Classification D OMIM : 600721 236792 613657 615182 DiseasesDB : 34515 SNOMED CT : 698870008 External resources Orphanet : 19 v t e Inborn error of amino acid metabolism K → acetyl-CoA Lysine /straight chain Glutaric acidemia type 1 type 2 Hyperlysinemia Pipecolic acidemia Saccharopinuria Leucine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency 3-Methylglutaconic aciduria 1 Isovaleric acidemia Maple syrup urine disease Tryptophan Hypertryptophanemia G G→ pyruvate → citrate Glycine D-Glyceric acidemia Glutathione synthetase deficiency Sarcosinemia Glycine → Creatine : GAMT deficiency Glycine encephalopathy G→ glutamate → α-ketoglutarate Histidine Carnosinemia Histidinemia Urocanic aciduria Proline Hyperprolinemia Prolidase deficiency Glutamate / glutamine SSADHD G→ propionyl-CoA → succinyl-CoA Valine Hypervalinemia Isobutyryl-CoA dehydrogenase deficiency Maple syrup urine disease Isoleucine 2-Methylbutyryl-CoA dehydrogenase deficiency Beta-ketothiolase deficiency Maple syrup urine disease Methionine Cystathioninuria Homocystinuria Hypermethioninemia General BC / OA Methylmalonic acidemia Methylmalonyl-CoA mutase deficiency Propionic acidemia G→ fumarate Phenylalanine / tyrosine Phenylketonuria 6-Pyruvoyltetrahydropterin synthase deficiency Tetrahydrobiopterin deficiency Tyrosinemia Alkaptonuria / Ochronosis Tyrosinemia type I Tyrosinemia type II Tyrosinemia type III / Hawkinsinuria Tyrosine → Melanin Albinism : Ocular albinism ( 1 ) Oculocutaneous albinism ( Hermansky–Pudlak syndrome ) Waardenburg syndrome Tyrosine → Norepinephrine Dopamine beta hydroxylase deficiency reverse: Brunner syndrome G→ oxaloacetate Urea cycle / Hyperammonemia ( arginine aspartate ) Argininemia Argininosuccinic aciduria Carbamoyl phosphate synthetase I deficiency Citrullinemia N-Acetylglutamate synthase deficiency Ornithine transcarbamylase deficiency / translocase deficiency Transport / IE of RTT Solute carrier family : Cystinuria Hartnup disease Iminoglycinuria Lysinuric protein intolerance Fanconi syndrome : Oculocerebrorenal syndrome Cystinosis Other 2-Hydroxyglutaric aciduria Aminoacylase 1 deficiency Ethylmalonic encephalopathy Fumarase deficiency Trimethylaminuria v t e Medicine Specialties and subspecialties Surgery Cardiac surgery Cardiothoracic surgery Colorectal surgery Eye surgery General surgery Neurosurgery Oral and maxillofacial surgery Orthopedic surgery Hand surgery Otolaryngology ENT Pediatric surgery Plastic surgery Reproductive surgery Surgical oncology Transplant surgery Trauma surgery Urology Andrology Vascular surgery Internal medicine Allergy / Immunology Angiology Cardiology Endocrinology Gastroenterology Hepatology Geriatrics Hematology Hospital medicine Infectious disease Nephrology Oncology Pulmonology Rheumatology Obstetrics and gynaecology Gynaecology Gynecologic oncology Maternal–fetal medicine Obstetrics Reproductive endocrinology and infertility Urogynecology Diagnostic Radiology Interventional radiology Nuclear medicine Pathology Anatomical Clinical pathology Clinical chemistry Cytopathology Medical microbiology Transfusion medicine Other Addiction medicine Adolescent medicine Anesthesiology Dermatology Disaster medicine Diving medicine Emergency medicine Mass gathering medicine Family medicine General practice Hospital medicine Intensive care medicine Medical genetics Narcology Neurology Clinical neurophysiology Occupational medicine Ophthalmology Oral medicine Pain management Palliative care Pediatrics Neonatology Physical medicine and rehabilitation PM&R Preventive medicine Psychiatry Addiction psychiatry Radiation oncology Reproductive medicine Sexual medicine Sleep medicine Sports medicine Transplantation medicine Tropical medicine Travel medicine Venereology Medical education Medical school Bachelor of Medicine, Bachelor of Surgery Bachelor of Medical Sciences Master of Medicine Master of Surgery Doctor of Medicine Doctor of Osteopathic Medicine MD–PhD Related topics Alternative medicine Allied health Dentistry Podiatry Pharmacy Physiotherapy Molecular oncology Nanomedicine Personalized medicine Public health Rural health Therapy Traditional medicine Veterinary medicine Physician Chief physician History of medicine Book Category Commons Wikiproject Portal Outline
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Arteriosclerosis
Wikipedia
External links [ edit ] Classification D ICD - 10 : I25.0 , I25.1 , I70 MeSH : D001161 DiseasesDB : 1039 v t e Cardiovascular disease (vessels) Arteries , arterioles and capillaries Inflammation Arteritis Aortitis Buerger's disease Peripheral artery disease Arteriosclerosis Atherosclerosis Foam cell Fatty streak Atheroma Intermittent claudication Critical limb ischemia Monckeberg's arteriosclerosis Arteriolosclerosis Hyaline Hyperplastic Cholesterol LDL Oxycholesterol Trans fat Stenosis Carotid artery stenosis Renal artery stenosis Other Aortoiliac occlusive disease Degos disease Erythromelalgia Fibromuscular dysplasia Raynaud's phenomenon Aneurysm / dissection / pseudoaneurysm torso : Aortic aneurysm Abdominal aortic aneurysm Thoracic aortic aneurysm Aneurysm of sinus of Valsalva Aortic dissection Aortic rupture Coronary artery aneurysm head / neck Intracranial aneurysm Intracranial berry aneurysm Carotid artery dissection Vertebral artery dissection Familial aortic dissection Vascular malformation Arteriovenous fistula Arteriovenous malformation Telangiectasia Hereditary hemorrhagic telangiectasia Vascular nevus Cherry hemangioma Halo nevus Spider angioma Veins Inflammation Phlebitis Venous thrombosis / Thrombophlebitis primarily lower limb Deep vein thrombosis abdomen Hepatic veno-occlusive disease Budd–Chiari syndrome May–Thurner syndrome Portal vein thrombosis Renal vein thrombosis upper limb / torso Mondor's disease Paget–Schroetter disease head Cerebral venous sinus thrombosis Post-thrombotic syndrome Varicose veins Gastric varices Portacaval anastomosis Caput medusae Esophageal varices Hemorrhoid Varicocele Other Chronic venous insufficiency Chronic cerebrospinal venous insufficiency Superior vena cava syndrome Inferior vena cava syndrome Venous ulcer Arteries or veins Angiopathy Macroangiopathy Microangiopathy Embolism Pulmonary embolism Cholesterol embolism Paradoxical embolism Thrombosis Vasculitis Blood pressure Hypertension Hypertensive heart disease Hypertensive emergency Hypertensive nephropathy Essential hypertension Secondary hypertension Renovascular hypertension Benign hypertension Pulmonary hypertension Systolic hypertension White coat hypertension Hypotension Orthostatic hypotensionNOS3, APOE, KL, SERPINA1, IL1B, PPARG, GSTA4, APOA1, MMP9, LMNA, CCL5, KDR, VCAN, ABCG5, LOX, MMP14, RELA, TBXA2R, LIPE, TBXAS1, NDUFS6, ITGA7, LIPA, HS3ST1, SMARCAL1, PCSK9, SLC5A2, FGF21, CCR5, POLDIP2, NR1I2, IL17A, IL18, CCL2, IL10, CXCL8, IL6, CAV1, CRK, CRP, MAPK14, SAA1, IL1A, APOM, SMUG1, CHI3L1, RNF19A, SCARB1, CD40, CD40LG, CD14, LGALS3, LEP, RETN, LDLR, GRAP2, LIPG, ADIPOQ, LCAT, KLF4, LPA, CXCL12, LPL, CDKN2A, XPR1, CETP, SELP, CD36, CX3CL1, PIK3CB, CST3, ERCC4, EGR1, GLP1R, TNF, ELN, MIR126, TP53, HSPA14, GCG, GABPA, ANGPTL4, ERCC2, PIK3CA, ERCC3, ERCC5, TLR4, ESR1, MIR21, MIR155, FN1, F3, VWF, TNFSF4, FABP4, FOXP3, UCP2, NOX4, VCAM1, VEGFA, TM7SF2, EDN1, SPP1, ANGPTL3, SREBF2, ABCG1, IGF1, IFNG, ICAM1, CX3CR1, CYBA, HSPD1, TET2, PLA2G10, STAT3, HP, IL37, HMOX1, TLR2, MIR33A, HMGB1, HIF1A, ACE, DECR1, FGF23, TGFB1, AIMP2, PLA2G7, DNMT1, DPP4, THBS1, CXCR4, MBL2, SELE, PLG, PRKAB1, AGER, PTGS2, ADAMTS7, PLA2G1B, PTX3, MTHFR, ACE2, NLRP3, PIK3CG, CXCL16, ANGPT2, PIK3CD, MPO, ANGPT1, MAPK1, SORT1, PLA2G2A, PON2, NR1H3, APOB, APOA4, APOC3, PLTP, APOA2, SERPINE1, NFE2L2, LPAL2, IL33, PON1, PPARA, ABCC6, KLF2, UTS2, MMP12, MOK, PECAM1, ALOX15, PRKAA2, OLR1, ALB, SIRT1, TNFRSF11B, VPS51, AGT, MEFV, AKT1, AGTR1, PRKAA1, ABCA1, CCR2, AHSA1, AHSG, ALOX5, PAPPA, MMP2, APOA5, MMP3, CDKN2B-AS1, REN, EDNRA, CHDH, CD44, GJA4, HAMP, CXCR6, MALAT1, MIR145, TNFRSF9, GPR162, TXN, PPIA, NPY, LRP1, MTCO2P12, CIMT, SOST, COX2, ACTB, MAPK3, ANPEP, TNC, CTSS, MIR221, ALDH2, EHMT1, SLC2A1, MMP1, MYD88, MIR223, CCN2, IL23A, GSTM1, PON3, ADAM17, APOL1, CAD, IL4, WNT5A, CASP1, USF1, PADI4, BSG, ACAT1, CD68, ZGLP1, BCL2, ATM, CLU, ESR2, MTOR, PPARD, ITGAX, INSR, MIR146A, APOH, FGF2, NR4A1, NR3C2, AKR1B1, RENBP, TSPO, HDAC9, TCF7L2, HGF, MFAP1, PTPN22, CSF2, ACKR3, LTA, BECN1, GDF15, MIR27A, S100A12, ROS1, CD34, STAT1, APRT, FOXO1, ABCB6, HSPB3, COPD, SFTPD, SGMS2, ADRA2B, HSPB2, SOAT1, HSPB1, PLB1, LCN2, NAMPT, YWHAZ, BGLAP, F2RL1, ADRA1A, TRAF6, F11R, GPR42, FTO, HPSE, PLAT, SSTR4, GSTT1, SELPLG, IFNA1, SOCS3, RARRES2, FCGR3A, LPAR2, PLPP3, LGMN, IL2RA, BGN, TFEB, CNR2, APLN, ITGB2, PTH, SQSTM1, JAK2, MMP13, IFNA13, BRS3, CAT, TFPI2, TFPI, CLOCK, HMGCR, SAA2, ALOX5AP, TREM1, MGP, HSD11B1, HSPA4, GAS5, KNG1, FMO3, CCL11, FOXO3, PDGFD, PGF, MYDGF, ACTRT1, DAB2IP, DHX40, UCP1, ISG20, PDE4D, NOD2, HFE, GRN, GPX1, TIMP1, NT5E, P2RX7, MIRLET7G, HSPG2, MAPK8, C1QTNF9, P2RY2, GNB3, NOTCH1, MIR122, NOS2, SREBF1, NOS1, CCN1, TUG1, ABCG8, PTEN, FCGR3B, ADIPOR1, CHIT1, MAGI2, ADM, TNFSF10, CAMP, MIR217, AOC3, AHR, CTNNB1, AIF1, ALOX15B, EGFR, SIRT3, ARL6IP1, CYBB, EPRS1, WDR1, ECE1, PLA2G6, PDCD6IP, MIR34A, PGR-AS1, TOR2A, MMRN1, BIRC3, ABI2, MIR29A, APP, CASP3, ARG1, ABO, EZH2, NTN1, F2R, F2, VLDLR, CCR7, CD1D, IL23R, HPGDS, RNR2, DKK1, MIR590, CYP2C9, CYP27A1, NR1H4, HSPA5, RBP4, MYOCD, SGSM3, ANGPTL8, PTGS1, TCF21, CFH, PTGIR, ARNTL, DNER, SLC33A1, CDKN2B, CD59, CHRM3, MIR30C1, IL32, CES1, CD163, NUP62, MAP4K4, CD47, LTB4R, S100A8, CBS, CASR, IRAK1, SCD, INS, CP, IDO1, SMPD1, ADAMTS4, IL13, OR10A4, TNFSF12, COMP, IL9, IRS2, BMP2, ENTPD1, IL17D, RYR3, DDR1, SOCS1, MAP3K5, IL27, MFGE8, CTH, MIF, TRIB3, PHACTR1, SLC9A1, LRP6, KLF14, MSR1, TERT, P4HB, PPARGC1A, GAS6, DCTN4, PARP1, FURIN, GCH1, TLR7, PLIN2, APLNR, GH1, GHSR, GJA1, TNFRSF1A, ELAVL2, EPHB2, EPHX2, CBSL, TNFRSF4, KHDRBS1, VIM, SERPINF1, ACLY, MIR19B1, TNFSF13B, F10, ADIPOR2, FLNA, FLT1, MIR17, PKM, FPR2, MIR210, VKORC1, TNFRSF12A, MIR30C2, IL19, TIMP3, IL25, LPCAT3, CXCL1, MIR24-1, GTF2H1, THBD, CNBP, S1PR1, SIRT6, AQP1, YAP1, MIR33B, ADD1, ADAM10, CCL4, PLAU, SP6, MYC, LTA4H, PTPN1, CD5L, ADAM8, AOC2, MERTK, PROS1, ESAM, SLC35A1, PF4, GPBAR1, CCL22, NFKB1, APOBEC1, PDZK1, MYLK, OGA, LEPR, PIN1, NISCH, LIPC, MAP2K1, SCAP, ANXA1, PNPLA2, NPPB, APOA1-AS, ANGPTL2, B2M, NOS1AP, SEMA6A, MRC1, JCAD, TP53COR1, CA2, BTF3P11, KLF5, IL1F10, PCLAF, BMP4, NPPC, MMP8, ANXA5, ROCK1, CAPN10, S100A9, GAL3ST1, MTTP, S100B, PRDX1, LINC01672, PSRC1, SMAD3, MAOA, ADAMTS13, MAS1, MAZ, CST12P, COX1, SLC25A20, AR, MT2A, TRPV4, VDR, HABP2, IKBKB, LRP8, IGF1R, CASZ1, GIP, MSTN, STC2, GSK3B, NR4A3, MIR216A, ENG, IL6ST, CRISP2, XDH, IL1RN, TAGLN, SLC52A1, MIR377, SORL1, GC, MIR98, ELK1, SYK, CTSD, HCAR2, MIR222, DYM, GPI, TIE1, SEMA7A, TNFSF12-TNFSF13, HSP90AA1, MIAT, TLR5, STAT4, EGF, CXADR, MIR10A, EPHA2, DUSP1, KIT, CTSK, ID3, ELANE, CYP2B6, SOD2, SOD1, VTN, MBTPS1, FSHMD1A, KIF6, EVPL, TTR, ITGB3, SERPIND1, F5, MIR20A, ITGA2B, FCGR2A, SHBG, FABP5, ACSL1, PTK2B, MIR19A, FBN1, MIR497, CREG1, SETD2, MIR212, MIR144, XBP1, IL15, HLA-C, RMC1, ADAM15, MIR143, NEAT1, DCN, MEG3, IRF1, ATN1, BATF3, IRF6, THBS4, PRTN3, PDIA2, PADI1, GORASP1, TGM2, CLEC7A, NPC1L1, GHRL, PROC, ZFP36, POU2F3, TLR3, PLXNA2, VCL, MBL3P, NFAT5, TUFM, NOXA1, TMED7, PLA2G4A, TRPC3, IRAK4, WRN, PLIN1, NOD1, NOX5, MAPK7, ELOVL6, COPS5, RIPK3, GDF11, TNFRSF1B, PPBP, ZC3HC1, PRG4, TRIM13, PRKAR1A, WNK1, XIST, ZMPSTE24, STK11, ZHX2, TNFSF14, RIPK2, SIGLEC1, SLC17A5, ADAMTS3, PLAAT1, TNFSF9, CCL4L2, GREM1, SNAI2, NCOR1, S100A1, RXRA, RPS19, PDE5A, AS3MT, AHRR, HSPB8, ROCK2, NR2F2, ST3GAL4, SFRP5, TBX18, LDB2, AIMP1, PLA2G15, CH25H, CCL21, ACSS2, IL27RA, AIM2, ABCA12, DEFB103B, CCL19, CCL18, HDAC3, SELENOS, NCEH1, SOX9, SPG7, SOX18, NR1I3, SOAT2, STAT6, LOH19CR1, NIF3L1, HDAC5, SYT1, TLR9, TNFSF11, RGCC, KLRK1, TAM, TEK, PTGDS, PTAFR, TFAP2A, TNFSF15, RAG1, PALLD, RARA, SRI, NOX1, RNF213, FOXP1, DKK3, PALD1, ST2, RAPGEF5, PIEZO1, INTU, PMPCA, MPRIP, RCN2, NAAA, KDM6B, LDLRAP1, POSTN, FOS, BRCA1, IGF2, CEL, CTSC, FFAR4, IRF8, CHGA, HSPA1A, HRH2, CHRNA4, CISH, HRH1, CLIC1, HNF4A, NANOS3, HMGA1, IRGM, NRG1, CCR3, TICAM2, MIR146B, IRF2BP2, HDAC1, GSTK1, NEXN-AS1, MIA3, GZMB, GUCY1A1, CMKLR1, CNN2, IGFBP1, IGFBP7, GPIHBP1, NCF1, LRP2, LPP, C3, LIF, LGALS3BP, MIR652, RPSA, CCDC80, CAPN1, CAST, CASP9, CD28, PRSS55, CD69, MIR499A, CXADRP1, UCA1, MIR30E, CDH5, IRS1, IRF5, INPP5D, CXCL10, CXCR2, CDKN1A, IL6R, IL5, CDKN1B, CNP, CCL4L1, CNR1, HBEGF, MIR148B, MIR135B, MIR133B, MIR206, ERG, EPO, EPHA1, CTSL, CYP1A1, LPAR1, EDA, CYP1A2, PLIN5, DSPP, CTF1, MIR23B, DEFB103A, DSC1, DNASE1, DNAH8, MIR25, CYP2J2, MIR99A, MIR29B1, CYP3A5, MIR29B2, CYP7A1, CYP19A1, F13A1, FBN2, C1QL3, COX8A, CXCL2, NR3C1, GPER1, MIRLET7B, COL4A1, GOT2, GLO1, MIR10B, GJA5, GHRHR, COL15A1, COMT, MIR134, MIR142, FCGR2B, CR1, GATA2, GAST, MIR150, MIR152, FOLR2, MIR181A2, MIR375, FGG, FGFR1, FGF13, FGF1, FGB, C1QBP, DAB2, BMP7, LINC-ROR, HAVCR2, LARP1BP2, ACAN, GFM1, TSLP, JAG1, AGTR2, NEU1, AKT2, NEXN, MYH11, ORMDL3, EARS2, MIR4463, RHOA, ARR3, MSRA, KLRC4-KLRK1, TXNIP, SNHG16, C1QTNF6, TNFRSF13C, MMP7, FOXO4, RNU6-392P, CCN3, ADTRP, NPPA, ENPP1, H3P31, ABCA4, PDGFA, ADAM33, COL18A1, ACP3, SESN2, PAEP, PCSK6, ARID5B, HHIPL1, OSM, LOC107985770, RN7SL263P, KISS1R, OGN, OGG1, SPZ1, ADK, ACCS, ADRB2, NPR3, TMED7-TICAM2, APC, MCAM, SLCO6A1, SMAD7, OSCAR, MAA, MC1R, OSCP1, BCR, HLP, HOTAIR, MIR338, MIR612, MIR335, HBP1, MLC1, USP20, NNT, MIR342, FETUB, MIR370, MMD, MIR330, MIR647, MALT1, RNU1-1, MIR378A, DDAH2, MIR451A, HNP1, MIR431, MIR18B, PCOLCE2, BRD8, MIR362, H4C15, ATP6V0A2, SLC16A8, MIR449A, PIK3R5, HAVCR1, LILRB1, SIRT1-AS, MIR664A, CLCF1, H3P28, DCTN6, CTCF, MCF2L, MIR17HG, KCNH4, H3P23, SIGLEC9, IL17B, MIR410, TLX1NB, PDCD4, RBMS3, MIR758, CAMKK2, BHLHE22, SASH1, SFTPA2, LNCRNA-ATB, LINC02605, TRAM1, NBEAL2, FRS2, SRRM2, GSC-DT, MASCRNA, POTEF, CCR9, SEPTIN9, PACS2, CYSLTR1, CES3, MTHFD2, NES, SLC39A1, TRAF3IP2, MIR328, NME1-NME2, MIR575, PART1, MICA, BACE1, POT1, CLIC4, WWTR1, LEF1-AS1, DAPK2, CARD8, ECSCR, PNKD, ADGRA2, CHMP2B, MIR494, MICOS10-NBL1, TMEM98, MIR455, CASC11, MGLL, SIRT2, AAA1, EID1, MYH15, PANX1, P2RX2, MIR505, ZNF318, MIR3188, OCLN, FIQTL1, MIR519D, MIR486-1, GCA, LMOD1, BAMBI, P2RX5-TAX1BP3, APPL1, EBNA1BP2, CDR1-AS, STAB1, MIR222HG, MIR876, ESM1, CLEC4E, MIR489, FBXO8, FBXO3, KERA, ABHD2, PLA2G2D, DDAH1, SFTPA1, LILRB4, DEFB4B, C20orf181, CARHSP1, ACOT7, ADAMTS5, MIR492, NORAD, HOXA-AS3, COPE, ARHGEF26, SNF8, HIF1A-AS1, SLC2A6, PSS, MIR490, GATD3B, PATZ1, TES, LOC102724197, CIT, CLEC5A, PPP1R3B, IGLV2-18, TDRD9, MAGEC3, CD248, DCBLD2, KCNH8, TMEM18, JPH3, PODN, TNFAIP8L1, STRIP2, SLC5A10, MRTFA, CIP2A, GPR119, H4-16, PRAP1, MARK4, CCAR2, TADA1, C1QTNF5, SLAMF7, NGB, C1QTNF1, OSBPL1A, CYGB, MAGEE2, ZBTB46, IL17F, PDIK1L, MARCHF10, PDGFC, LINC00599, AMOT, TRPV5, BTLA, LTB4R2, CYP26B1, SLC2A9, SUCNR1, BPIFB4, IL34, TRPM6, SLC2A4RG, NRG4, SPHK2, LGALS14, PWAR1, ANKS1B, PNO1, FAM20C, SERPINA12, SIRPA, TBX20, IL21, SIGIRR, ADAMTS18, MFRP, UBE2Z, RASL11B, MAK16, METRN, LCOR, KCTD15, AKT1S1, MINDY4, CCDC8, TAF3, FA2H, ARHGAP24, PINK1, PLA2G12A, SLC52A2, COLEC12, APOL6, SPX, PNPLA3, NAA25, HMBOX1, TNFAIP8L2, RHBDF2, ADM2, RETNLB, CREB3L3, EGLN3, CARD9, SENP2, MUC16, CLEC6A, CELA2A, CIDEC, ARHGAP18, SAMSN1, SLC39A8, CACNA2D4, GGTLC1, WDR20, RSAD2, AGXT2, ROBO3, DPP9, SAMD1, WNT3A, ARHGEF28, FBRS, DCLK3, ABCC11, HSH2D, ORAI1, P2RY12, PAQR7, PAOX, IGKV2D-29, PLEKHO1, TRAT1, MIR182, MIR18A, MIR15A, STEAP4, MLXIPL, MIR149, MIR148A, INSIG2, EGFL7, MIR140, MIR136, MIR185, GP6, MZB1, TLR8, MIR127, MIR125A, MIR107, MIR100, SIRT7, LINC01194, HACD4, SNX19, MIR183, IL22, TBPL2, HILPDA, MIR302A, KLF15, MIR29C, PYCARD, BRD7, CD274, SENP1, ICOS, MIR296, MIR28, MIR27B, OSGIN1, IL20, MIR23A, MIR224, MIR22, MIR214, MIR205, PSAT1, SLC40A1, MIR199A2, MIR199A1, MIR192, MIR188, C1QTNF12, UFM1, APOBR, LRP2BP, ATG16L1, SCARA5, HCCAT5, RCBTB1, CLEC9A, H19, CSGALNACT2, SMPD3, SOX6, NSUN5, SGMS1, ADCY10, S100A7A, FNDC5, LINC00305, CISD1, ZEB1-AS1, MPEG1, HYLS1, UNC5B, KMT2E, ZC4H2, TET3, MLKL, MOCOS, CLEC4D, NBAS, TOLLIP, ENHO, INPP5K, TM6SF2, PTOV1, P2RY13, FCRL6, NANS, GOLGA6A, ACER2, ARSI, LINC00299, KRT20, MMS, SMOX, DLL4, ARMH1, BRINP3, NANOS2, ENPP7, SAMD9, PGPEP1, DPP8, CDKAL1, TESC, A2M, STAR, HEXIM1, LBR, ITGAM, ITGAL, ITGAE, ITGAD, ITGA5, ITGA2, IRF3, IRF2, ILK, IL11, IL7, IL2, IGSF1, IGHG3, IGHE, IGFBP5, IGF2R, ITGAV, ITGB4, ITIH4, KCNMB1, LAIR1, LAG3, LAD1, KPNA4, KPNA3, KLK1, KISS1, KCNJ11, ITPR1, JUP, JUND, JUNB, JUN, IVD, ITPR3, ITPR2, IFI27, IDH2, ID1, GP1BA, GSR, GPX4, GPT, FFAR1, GPR39, LPAR4, CXCR3, GOLGB1, GTF3A, GLRX, GLI2, GCLM, GFER, GDF2, NR6A1, GCKR, GSTM2, GTS, HSPA2, FOXA3, HSPA1B, HSF1, HES1, HPX, HOXB9, HOXA1, HNRNPU, HLA-B, GYPC, HLA-A, HDLBP, HDC, HCRT, HAS3, HAS2, HAL, LBP, LDHA, PCDH8, LECT2, NOTCH2, NOP2, NNMT, NME2, NINJ2, NGFR, NFKBIA, NFKB2, NFE2, NFIA, NF1, NEDD4, NDUFA2, NCF2, NBN, NBL1, NAGLU, NOTCH4, PNP, NPHP1, P2RX3, CNTN3, PAK1, PAH, PEBP1, P2RY1, P2RX5, P2RX4, P2RX1, SLC11A2, OSBP, SLC22A18, OPRK1, DDR2, ROR2, YBX1, NRF1, MYH9, MUC1, TRNL2, SMAD1, MDK, SMCP, CD46, MCM3, MCL1, MC4R, SMAD2, LYZ, MECP2, CD180, LUM, LTB, LSAMP, LRP5, LMNB1, FADS1, MDM2, MEF2A, TRNL1, ABCC1, MTRR, RNR1, CYTB, MTAP, MT1F, MST1R, MST1, MPV17, MEF2C, MMP17, MMP11, MMP10, KMT2A, MAP3K10, CXCL9, CD99, GCK, GCGR, GATA4, LRRC32, CD19, KRIT1, RUNX2, CAPG, CANX, CALU, CALR, CACNA1C, CA1, SERPING1, BLM, PRDM1, BIK, CEACAM1, BDKRB2, BCL3, CCND1, MS4A1, CD27, CD80, CEBPA, COL1A2, CCR8, CCR6, CMA1, CLCN2, LYST, CEBPB, CDKN1C, CD70, CDK9, CDK5, CDK2, CDC42, CD151, CD81, CD74, BAX, AZU1, AZGP1, ADCY9, AHCY, NR0B1, AGRP, AP2A1, ADRB3, ADH5, ADCYAP1, ADCY8, ALOX12, ADA, ACTA2, ACP5, ACP1, ACACA, ABR, SERPINA3, ALCAM, ALPL, ATP7A, STS, ATP2B1, ATOX1, ATOH1, ATIC, ATF4, ASS1, ARSL, ARSB, AMH, FAS, KLK3, APOC2, XIAP, APEX1, APCS, ANXA2, CORT, CPB2, CLDN7, EPAS1, FABP3, FABP2, F12, F11, ETS1, ERN1, EREG, EMP1, FAT1, MARK2, EFNB1, EEF1B2P2, EDN3, TYMP, EBF1, DUSP5, FAP, FBLN2, DNMT3B, FOSB, FYN, ACKR1, FUT8, FUT7, FUT3, FTH1, NR5A2, FMOD, FDPS, FLT4, FOXM1, VEGFD, FHL2, FGFR4, FGF12, FGA, RCAN1, DMRT1, CPOX, CSF2RB, CTSG, CTSB, CTPS1, CTNND1, CTBS, NKX2-5, CSF3, CSF1R, CYP2C19, CSF1, CRYGD, CRY1, CRMP1, ATF2, CREB1, CPT2, CYLD, CYP2C8, DMD, GADD45A, DLD, DIO2, NQO1, DHCR24, DHCR7, DEFB4A, DDIT3, DBP, CYP2D6, DBN1, BRINP1, DAG1, CYP27B1, CYP26A1, CYP3A4, CYP2E1, PC, PCNA, PDLIM5, FADS2, PHOX2B, TIMELESS, SGPL1, SPHK1, VNN1, ALKBH1, HCAR3, CCN5, NRP1, SUCLA2, TNFRSF11A, TNFRSF6B, ADAM9, TNFSF13, DGAT1, VAMP8, DYNLL1, TRPA1, KALRN, ARTN, OSMR, PPIG, SLIT2, GPR55, COPB2, PDLIM7, MAGI1, ARHGEF2, IL1RL1, PSTPIP2, TMSB10, HGS, PDCD5, ARHGEF1, P2RX6, SLC16A3, CLDN1, TP63, PLA2G4C, DENR, SCG2, NRIP1, SLC7A5, HMGA2, AAAS, KMT2D, ADAM12, ARHGEF5, FZD5, KDM5D, NPHS2, ZNF202, ZNF148, TRPV1, BEST1, VIP, VAV2, GATD3A, H4C9, CYP4F2, H4C5, HAT1, PIK3R3, PPM1D, RGS5, NR0B2, H4C14, H4C13, H4C2, BRAP, H4C8, H4C3, H4C11, H4C12, H4C6, H4C4, H4C1, COX5A, ABCG2, PCOLCE, GSTO1, TLR6, LANCL1, TCIRG1, SPEG, STUB1, FSTL3, RAMP1, SPRY1, RABEPK, KLRG1, MPZL2, PSME3, PRMT3, SORBS3, ATP6AP2, TRIM28, EBI3, MICU1, DLC1, PEMT, KAT5, TXNRD2, CXCL13, HTATIP2, PRDX4, PROCR, ZNRD2, ATG7, SEMA4D, SPON2, STK25, CREB3, CAP1, FST, VAV3, C1D, LYPLA1, G3BP1, ZNF263, IL18BP, GOSR2, DOCK4, SEMA3E, ECE2, KDM4A, PHF14, TRAF4, AKAP12, H6PD, ATG13, CXCL14, PTGES, NPEPPS, ADAMTS1, ATG5, CHST3, PCYT1B, KMT2B, MTSS1, DNM1L, RCE1, SLC17A4, PARP3, SH2B3, HDAC6, AKT3, SCO2, KCNE2, FGF19, BMS1, MVP, DLEC1, MAFB, MFN2, ELMO1, TRIM14, MAML1, VAV1, UTRN, UMOD, SUMO1, RFC2, RASGRF1, RASA1, RARB, RAG2, RAC2, RAC1, NECTIN2, NECTIN1, PVR, PTPRF, PTPN11, PTPN6, PTPN2, PTN, PTHLH, PTGIS, RFX1, RFX5, RGS1, S100A7, CCL3, CCL1, SCP2, SCN7A, SAT1, TSPAN31, SAA3P, RPS6KA1, RGS2, RORA, RNASE3, RNASE1, RLN2, RHEBP1, RGS7, RGS3, PTGER3, PTBP1, PSMD9, PDK4, PLAG1, PITX3, PITX2, PIP, SERPINB9, PGC, SLC26A4, PDK1, PRRX1, PDGFRB, PDGFB, PDE4A, PCSK5, PCSK1, PCP4, PCOS1, SERPINF2, PODXL, PSMD7, MAPK9, PSMC5, PSMB8, PSMA6, RELN, PROX1, PRNP, MAP2K7, PRKCB, POMC, PRKCA, PREP, PTPA, PPP2R2A, PPP1R1A, MED1, POU2F1, CCL7, CCL8, CCL17, TRBV20OR9-2, THY1, THM, TGFB2, TGFB1I1, TFRC, TFAM, TDO2, TCF15, TNFAIP6, ZEB1, HNF1A, TAZ, MAP3K7, TAC1, ABCC8, SULT2A1, TLR1, TNNI3, STIM1, TRL-TAG1-1, TYROBP, TXNRD1, TWIST1, TSC1, TRPC6, TRPC5, TRPC1, TRAF2, TP73, TRAF1, HSP90B1, TPT1, TPO, TPM2, TPI1, TPH1, AURKA, NAT2, CCL20, SGCB, SLC12A3, SLC8A1, SLC6A8, SLC3A2, SKP2, ST6GAL1, SHC1, SRSF2, SLPI, SRSF1, SFRP4, SELL, SDC4, SDC1, CCL25, CCL23, SLC22A1, SMARCA4, ST14, SPARC, SSTR2, SST, SSRP1, SSBP1, TRIM21, SRY, SPI1, SP1, SMN1, SOS1, SOD3, SNTB2, SNAI1, SMS, SMPD2, SMN2, H3P10
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Omphalitis Of Newborn
Wikipedia
External links [ edit ] Classification D ICD - 10 : P38 ICD - 9-CM : 771.4 DiseasesDB : 34512 External resources eMedicine : ped/1641 v t e Conditions originating in the perinatal period / fetal disease Maternal factors complicating pregnancy, labour or delivery placenta Placenta praevia Placental insufficiency Twin-to-twin transfusion syndrome chorion / amnion Chorioamnionitis umbilical cord Umbilical cord prolapse Nuchal cord Single umbilical artery presentation Breech birth Asynclitism Shoulder presentation Growth Small for gestational age / Large for gestational age Preterm birth / Postterm pregnancy Intrauterine growth restriction Birth trauma scalp Cephalohematoma Chignon Caput succedaneum Subgaleal hemorrhage Brachial plexus injury Erb's palsy Klumpke paralysis Affected systems Respiratory Intrauterine hypoxia Infant respiratory distress syndrome Transient tachypnea of the newborn Meconium aspiration syndrome Pleural disease Pneumothorax Pneumomediastinum Wilson–Mikity syndrome Bronchopulmonary dysplasia Cardiovascular Pneumopericardium Persistent fetal circulation Bleeding and hematologic disease Vitamin K deficiency bleeding HDN ABO Anti-Kell Rh c Rh D Rh E Hydrops fetalis Hyperbilirubinemia Kernicterus Neonatal jaundice Velamentous cord insertion Intraventricular hemorrhage Germinal matrix hemorrhage Anemia of prematurity Gastrointestinal Ileus Necrotizing enterocolitis Meconium peritonitis Integument and thermoregulation Erythema toxicum Sclerema neonatorum Nervous system Perinatal asphyxia Periventricular leukomalacia Musculoskeletal Gray baby syndrome muscle tone Congenital hypertonia Congenital hypotonia Infections Vertically transmitted infection Neonatal infection rubella herpes simplex mycoplasma hominis ureaplasma urealyticum Omphalitis Neonatal sepsis Group B streptococcal infection Neonatal conjunctivitis Other Miscarriage Perinatal mortality Stillbirth Infant mortality Neonatal withdrawal
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Robovirus
Wikipedia
Viral diseases transmitted by rodents [ edit ] One example of a robovirus is hantavirus , which causes hantavirus pulmonary syndrome . Humans can be infected with Hantavirus Pulmonary Syndrome through direct contact with rodent droppings, saliva, or urine infected with strains of the virus. ... Retrieved 30 October 2017 . v t e Zoonotic viral diseases (A80–B34, 042–079 ) Arthropod -borne Mosquito -borne Bunyavirales Arbovirus encephalitides : La Crosse encephalitis LACV Batai virus BATV Bwamba Fever BWAV California encephalitis CEV Jamestown Canyon encephalitis Tete virus Tahyna virus TAHV Viral hemorrhagic fevers : Rift Valley fever RVFV Bunyamwera fever BUNV Ngari virus NRIV Flaviviridae Arbovirus encephalitides : Japanese encephalitis JEV Australian encephalitis MVEV KUNV Saint Louis encephalitis SLEV Usutu virus West Nile fever WNV Viral hemorrhagic fevers : Dengue fever DENV-1-4 Yellow fever YFV Zika fever Zika virus Togaviridae Arbovirus encephalitides : Eastern equine encephalomyelitis EEEV Western equine encephalomyelitis WEEV Venezuelan equine encephalomyelitis VEEV Chikungunya CHIKV O'nyong'nyong fever ONNV Pogosta disease Sindbis virus Ross River fever RRV Semliki Forest virus Reoviridae Banna virus encephalitis Tick -borne Bunyavirales Viral hemorrhagic fevers : Bhanja virus Crimean–Congo hemorrhagic fever (CCHFV) Heartland virus Severe fever with thrombocytopenia syndrome ( Huaiyangshan banyangvirus ) Tete virus Flaviviridae Arbovirus encephalitides : Tick-borne encephalitis TBEV Powassan encephalitis POWV Viral hemorrhagic fevers : Omsk hemorrhagic fever OHFV Kyasanur Forest disease KFDV AHFV Langat virus LGTV Orthomyxoviridae Bourbon virus Reoviridae Colorado tick fever CTFV Kemerovo tickborne viral fever Sandfly -borne Bunyavirales Adria virus (ADRV) Oropouche fever Oropouche virus Pappataci fever Toscana virus Sandfly fever Naples virus Rhabdoviridae Chandipura virus Mammal -borne Rodent -borne Arenaviridae Viral hemorrhagic fevers : Lassa fever LASV Venezuelan hemorrhagic fever GTOV Argentine hemorrhagic fever JUNV Brazilian hemorrhagic fever SABV Bolivian hemorrhagic fever MACV LUJV CHPV Bunyavirales Hemorrhagic fever with renal syndrome DOBV HTNV PUUV SEOV AMRV THAIV Hantavirus pulmonary syndrome ANDV SNV Herpesviridae Murid gammaherpesvirus 4 Bat -borne Filoviridae BDBV SUDV TAFV Marburg virus disease MARV RAVV Rhabdoviridae Rabies ABLV MOKV DUVV LBV CHPV Paramyxoviridae Henipavirus encephalitis HeV NiV Coronaviridae SARS-related coronavirus SARS-CoV MERS-CoV SARS-CoV-2 Primate -borne Herpesviridae Macacine alphaherpesvirus 1 Retroviridae Simian foamy virus HTLV-1 HTLV-2 Poxviridae Tanapox Yaba monkey tumor virus Multiple vectors Rhabdoviridae Rabies RABV Mokola virus Poxviridae Monkeypox
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Human Monocytotropic Ehrlichiosis
Wikipedia
External links [ edit ] Classification D ICD - 9-CM : 082.41 MeSH : D016873 DiseasesDB : 31131 External resources MedlinePlus : 001381 eMedicine : med/3391 v t e Proteobacteria -associated Gram-negative bacterial infections α Rickettsiales Rickettsiaceae / ( Rickettsioses ) Typhus Rickettsia typhi Murine typhus Rickettsia prowazekii Epidemic typhus , Brill–Zinsser disease , Flying squirrel typhus Spotted fever Tick-borne Rickettsia rickettsii Rocky Mountain spotted fever Rickettsia conorii Boutonneuse fever Rickettsia japonica Japanese spotted fever Rickettsia sibirica North Asian tick typhus Rickettsia australis Queensland tick typhus Rickettsia honei Flinders Island spotted fever Rickettsia africae African tick bite fever Rickettsia parkeri American tick bite fever Rickettsia aeschlimannii Rickettsia aeschlimannii infection Mite-borne Rickettsia akari Rickettsialpox Orientia tsutsugamushi Scrub typhus Flea-borne Rickettsia felis Flea-borne spotted fever Anaplasmataceae Ehrlichiosis : Anaplasma phagocytophilum Human granulocytic anaplasmosis , Anaplasmosis Ehrlichia chaffeensis Human monocytotropic ehrlichiosis Ehrlichia ewingii Ehrlichiosis ewingii infection Rhizobiales Brucellaceae Brucella abortus Brucellosis Bartonellaceae Bartonellosis : Bartonella henselae Cat-scratch disease Bartonella quintana Trench fever Either B. henselae or B. quintana Bacillary angiomatosis Bartonella bacilliformis Carrion's disease , Verruga peruana β Neisseriales M+ Neisseria meningitidis/meningococcus Meningococcal disease , Waterhouse–Friderichsen syndrome , Meningococcal septicaemia M− Neisseria gonorrhoeae/gonococcus Gonorrhea ungrouped: Eikenella corrodens / Kingella kingae HACEK Chromobacterium violaceum Chromobacteriosis infection Burkholderiales Burkholderia pseudomallei Melioidosis Burkholderia mallei Glanders Burkholderia cepacia complex Bordetella pertussis / Bordetella parapertussis Pertussis γ Enterobacteriales ( OX− ) Lac+ Klebsiella pneumoniae Rhinoscleroma , Pneumonia Klebsiella granulomatis Granuloma inguinale Klebsiella oxytoca Escherichia coli : Enterotoxigenic Enteroinvasive Enterohemorrhagic O157:H7 O104:H4 Hemolytic-uremic syndrome Enterobacter aerogenes / Enterobacter cloacae Slow/weak Serratia marcescens Serratia infection Citrobacter koseri / Citrobacter freundii Lac− H2S+ Salmonella enterica Typhoid fever , Paratyphoid fever , Salmonellosis H2S− Shigella dysenteriae / sonnei / flexneri / boydii Shigellosis , Bacillary dysentery Proteus mirabilis / Proteus vulgaris Yersinia pestis Plague / Bubonic plague Yersinia enterocolitica Yersiniosis Yersinia pseudotuberculosis Far East scarlet-like fever Pasteurellales Haemophilus : H. influenzae Haemophilus meningitis Brazilian purpuric fever H. ducreyi Chancroid H. parainfluenzae HACEK Pasteurella multocida Pasteurellosis Actinobacillus Actinobacillosis Aggregatibacter actinomycetemcomitans HACEK Legionellales Legionella pneumophila / Legionella longbeachae Legionnaires' disease Coxiella burnetii Q fever Thiotrichales Francisella tularensis Tularemia Vibrionaceae Vibrio cholerae Cholera Vibrio vulnificus Vibrio parahaemolyticus Vibrio alginolyticus Plesiomonas shigelloides Pseudomonadales Pseudomonas aeruginosa Pseudomonas infection Moraxella catarrhalis Acinetobacter baumannii Xanthomonadaceae Stenotrophomonas maltophilia Cardiobacteriaceae Cardiobacterium hominis HACEK Aeromonadales Aeromonas hydrophila / Aeromonas veronii Aeromonas infection ε Campylobacterales Campylobacter jejuni Campylobacteriosis , Guillain–Barré syndrome Helicobacter pylori Peptic ulcer , MALT lymphoma , Gastric cancer Helicobacter cinaedi Helicobacter cellulitis v t e Tick-borne diseases and infestations Diseases Bacterial infections Rickettsiales Anaplasmosis Boutonneuse fever Ehrlichiosis ( Human granulocytic , Human monocytotropic , Human E. ewingii infection ) Scrub typhus Spotted fever rickettsiosis Pacific Coast tick fever American tick bite fever rickettsialpox Rocky Mountain spotted fever ) Spirochaete Baggio–Yoshinari syndrome Lyme disease Relapsing fever borreliosis Thiotrichales Tularemia Viral infections Bhanja virus Bourbon virus Colorado tick fever Crimean–Congo hemorrhagic fever Heartland bandavirus Kemerovo tickborne viral fever Kyasanur Forest disease Omsk hemorrhagic fever Powassan encephalitis Severe fever with thrombocytopenia syndrome Tete orthobunyavirus Tick-borne encephalitis Protozoan infections Babesiosis Other diseases Tick paralysis Alpha-gal allergy Southern tick-associated rash illness Infestations Tick infestation Species and bites Amblyomma Amblyomma americanum Amblyomma cajennense Amblyomma triguttatum Dermacentor Dermacentor andersoni Dermacentor variabilis Ixodes Ixodes cornuatus Ixodes holocyclus Ixodes pacificus Ixodes ricinus Ixodes scapularis Ornithodoros Ornithodoros gurneyi Ornithodoros hermsi Ornithodoros moubata Other Rhipicephalus sanguineus