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Growth Factors, Combined Defect Of
Omim
The microscopic changes in the skin were described by Mensing et al. (1982), who referred to the condition as a Werner-syndrome-like disorder. Biochemically, Hoepffner et al. (1989) demonstrated a combined defect in the action of 3 related peptides, insulin (176730), insulin-like growth factor I (147440) and epidermal growth factor (131530).
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Hemifacial Myohyperplasia
Omim
Lee et al. (2001) suggested that these cases represent a distinct entity and proposed that the syndrome be called hemifacial myohyperplasia.
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Calcific Aortic Disease With Immunologic Abnormalities, Familial
Omim
Aortic calcification is an important feature of the Singleton-Merten syndrome (182250), which is characterized also by dental dysplasia and osteoporosis and other bone changes.
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Progeroid Facial Appearance With Hand Anomalies
Omim
Clinical Features Giannotti et al. (1997) described a father and son with a progeroid syndrome characterized by an unusual facial appearance, sparse subcutaneous fat, and hand anomalies including syndactyly, camptodactyly, and clinodactyly ('finger deviation').
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Biliary Malformation With Renal Tubular Insufficiency
Omim
Lutz-Richner and Landolt (l973) described 2 male sibs with second-cousin parents and an identical syndrome leading to death at the age of about 4 months.
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Arthrogryposis, Distal, With Hypopituitarism, Mental Retardation, And Facial Anomalies
Omim
Rao et al. (2013) stated that their patient had features consistent with those in the sibs reported by Chitayat et al. (1990) and that their report extends the clinical phenotype of the disorder, which they called Chitayat-Hall syndrome. Inheritance Rao et al. (2013) stated that consanguinity in their family and affected sibs in the family reported by Chitayat et al. (1990) support autosomal recessive inheritance of the disorder.
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Progressive Disease
Wikipedia
Lungs : Emphysema due to alpha-1 antitrypsin deficiency is a slowly progressive pulmonary disease . Kidneys : Goodpasture's syndrome is a rapidly progressive glomerulonephritis , while diabetic glomerulosclerosis is slowly progressive.VEGFA, EGFR, KRAS, CD274, TP53, ERBB2, BRAF, TNF, ALK, CD38, LOC102723407, LOC102724971, IGHV3-69-1, AR, IL6, ZAP70, IL10, IL2, IGH, AFP, IGHV3OR16-7, MYCN, CEACAM5, BCL2, KLK3, PIK3CA, GINS2, IFNG, SMUG1, TGFB1, ABCB1, NRAS, CCL2, ESR1, EPHB1, CSF2, ELK3, IL4, ABL1, CFH, SLC6A2, SOD1, SST, CALCA, B2M, TYR, FOLH1, HSPA5, NR1H3, TBC1D9, SF3B1, IGHV1-69, RTEL1, MIR210, COPD, HLA-G, HLA-DRB1, MIR31, HLA-C, HGF, CFHR1, BCL2L11, IL18, GDF15, TTR, SCT, RET, PTGS2, STAT3, PDGFRB, NOTCH1, MS, IL15, MDM2, MCL1, PROM1, KDR, ITGA4, CXCL10, CCL5, LOC110806263, APOE, AREG, EGF, CD74, XIAP, DDT, AKT1, CTNNB1, RAPGEF5, CXCL13, HDAC4, AGR2, TIMM17A, TUBB4A, KLF2, MSLN, NR1I3, TRIM13, TENM1, PDPN, AVP, SCO2, ATM, ADAMTS13, HCP5, RIPK3, WIF1, NLRP1, DKK1, STS, FBXW11, ARRB1, ARR3, BACE1, SH3BP4, PRDX5, HAVCR1, EIF2AK1, APP, MDC1, FGFR3, TNFRSF17, TPM3, VCP, UBE2B, BMPR2, TYMS, BRCA1, TRPC5, TRAF6, TPI1, IGHV3-52, BTK, TSPO, TLR1, TK1, TIMP2, TH, TGFB2, BID, TRPV1, VWF, WNT5A, IL32, FCMR, MYOM2, CH25H, TIMELESS, CACNA1H, BCR, TNFRSF25, MIA, FGF23, ARHGEF5, OPLL, ALMS1, ZFP36, BDNF, PDLIM7, SETD2, HIPK2, C3orf35, MIR451A, MIR431, MIR34A, ALCAM, MIR224, MIR222, MIR221, ANGPT2, MIR21, MIR206, MIR200A, MIR19B1, MIR18A, MIR155, SLC35B2, MIR432, WIPF3, UCA1, GGTLC3, MTCO2P12, ALB, MIR4443, MIR1226, GGTLC4P, GGT2, MUC5B, CXADRP1, MIR613, MIR605, MIR592, MIR532, SNORD116@, GGTLC5P, GADL1, NANOS2, TGFA, S100A7A, CHPT1, ALLC, ATF7IP, ZNF654, FEV, DLL4, KRT20, CYCS, SPA17, BIRC3, IL23A, PLCE1, LINC00328, ING4, BIRC5, S100A14, TENM2, ANKRD36B, HAVCR2, ZAR1, BRAFP1, APCS, NLRP5, AZIN2, IL17F, CCDC54, IGAN1, CFHR5, PNPLA3, DHDDS, NOD2, VSIR, GAS5, CASR, TEK, TG, IRF1, ATN1, IL15RA, DSC3, DVL1, CXCL8, DVL2, IL4R, DVL3, TYMP, IL1RN, IL1R1, IL1B, IL1A, IGF1R, IFNGR2, SLC26A3, ITIH4, MLH1, DCX, KITLG, MEFV, MEF2C, CXADR, DNAJB9, CYP2A6, MC1R, LEPR, LEP, LCN2, LBR, STMN1, LAG3, KRT10, CYP17A1, IFNGR1, ELN, IDH1, ENO1, GRN, GPT, GP2, GNA12, GLI1, GLA, GGT1, GFAP, GEM, FSHMD1A, FXN, FES, FLT3LG, FLT3, VEGFD, GSTP1, HBB, FCGR3B, HLA-E, HSD17B2, HRAS, HPRT1, HPR, HMGB1, ERBB3, ERCC1, FCGR3A, HLA-DQB1, F2, HLA-B, HLA-A, HIF1A, FBN1, CXCL9, MMP2, TF, CCL18, CCL4, CDK4, CDK9, ATXN1, S100B, CDKN2A, RELB, RBBP8, RAD51, PTPRC, CEBPD, PSEN1, KLK6, PRL, MAP2K7, CDA, CCL19, MMP8, SDC1, FHIT, TRBV20OR9-2, TBX5, ADAM17, TAC1, SYK, CD1B, SSTR2, CD247, SPG7, MS4A1, SMPD1, SFTPD, SELE, SDHD, PRKAR1A, PPIA, POMC, PMS2, NTRK1, COX8A, CRH, NOS2, NFKBIA, NFKB1, NCAM1, CRP, MYC, MXI1, MUC1, MTX1, COX2, MRC1, MMP9, ROR1, OSM, PAH, PIK3CB, PMP22, ACTN4, PKD1, PIN1, PIK3CG, PIK3CD, CENPC, SERPINE1, SERPINA1, CHGA, PGR, PECAM1, CHI3L1, SERPINB2, PLP1
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Porokeratosis Plantaris Palmaris Et Disseminata
Orphanet
Differential diagnosis Differential diagnoses include other (genetic) punctate palmoplantar keratodermas such as acrokeratoelastoidosis of Costa, hyperkeratosis-hyperpigmentation syndrome, punctate palmoplantar keratoderma type 1 and hereditary papulotranslucent acrokeratoderma.
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Ichthyosis Hystrix Of Curth-Macklin
Orphanet
Differential diagnosis Differential diagnosis includes other forms of keratinopathic ichthyosis such as epidermolytic ichthyosis, as well as epidermolytic palmoplantar keratoderma, erythrokeratodermia variabilis, and KID syndrome (see these terms). Antenatal diagnosis Molecular prenatal diagnosis is available for affected families.
- Punctate Palmoplantar Keratoderma Type 1 Orphanet
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Familial Thrombocytosis
Orphanet
Differential diagnosis Differential diagnoses include causes of thrombocytosis with myeloproliferative neoplasm including chronic myeloid leukemia, polycythemia vera, primary myelofibrosis, sporadic or familial ET and myelodysplasic disorders with thrombocytosis including sideroblastic anemia or 5q- syndrome (see these terms), although these can be excluded by the presence of myeloproliferation.
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Endocapillary Proliferative Glomerulonephritis
Wikipedia
External links [ edit ] Classification D ICD - 10 : N00 - N08 with .4 suffix v t e Disease of the kidney glomerules Primarily nephrotic Non-proliferative Minimal change Focal segmental Membranous Proliferative Mesangial proliferative Endocapillary proliferative Membranoproliferative/mesangiocapillary By condition Diabetic Amyloidosis Primarily nephritic , RPG Type I RPG / Type II hypersensitivity Goodpasture syndrome Type II RPG / Type III hypersensitivity Post-streptococcal Lupus diffuse proliferative IgA Type III RPG / Pauci-immune Granulomatosis with polyangiitis Microscopic polyangiitis Eosinophilic granulomatosis with polyangiitis General glomerulonephritis glomerulonephrosis This article about a disease , disorder, or medical condition is a stub .
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Pleomorphic Lipoma
Wikipedia
External links [ edit ] Classification D ICD-O : 8854/0 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 tumor This Dermal and subcutaneous growths article is a stub .
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Nevi And Melanomas
Wikipedia
You can help Wikipedia by expanding it . v t e v t e Skin cancer of nevi and melanomas Melanoma Mucosal melanoma Superficial spreading melanoma Nodular melanoma lentigo Lentigo maligna / Lentigo maligna melanoma Acral lentiginous melanoma Amelanotic melanoma Desmoplastic melanoma Melanoma with features of a Spitz nevus Melanoma with small nevus-like cells Polypoid melanoma Nevoid melanoma Melanocytic tumors of uncertain malignant potential Nevus / melanocytic nevus Nevus of Ito / Nevus of Ota Spitz nevus Pigmented spindle cell nevus Halo nevus Pseudomelanoma Blue nevus of Jadassohn–Tièche Cellular Epithelioid Deep penetrating Amelanotic Malignant Congenital melanocytic nevus ( Giant Medium-sized Small-sized ) Balloon cell nevus Dysplastic nevus / Dysplastic nevus syndrome Acral nevus Becker's nevus Benign melanocytic nevus Nevus spilus
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Dissociative Disorder Not Otherwise Specified
Wikipedia
"Unspecified dissociative disorder" is given when the clinician doesn't give a reason. [1] The International Statistical Classification of Diseases and Related Health Problems (ICD-10) refers to the diagnosis as " Other dissociative and conversion disorders" . [2] Examples of DDNOS include chronic and recurrent syndromes of mixed dissociative symptoms, identity disturbance due to prolonged and intense coercive persuasion , disorders similar to dissociative identity disorder, acute dissociative reactions to stressful events, and dissociative trance. [1] DDNOS is the most common dissociative disorder and is diagnosed in 40% of dissociative disorder cases. [3] It is often co-morbid with other mental illnesses such as complex posttraumatic stress disorder , major depressive disorder , generalized anxiety disorder , personality disorders , substance use disorders , and eating disorders . [4] See also [ edit ] Psychology portal Psychiatry portal Biopsychiatry controversy Identity Jamais vu Memory Posttraumatic stress disorder References [ edit ] ^ a b American Psychiatric Association (2013).
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Muscle Tissue Neoplasm
Wikipedia
References [ edit ] External links [ edit ] Classification D ICD-O : 8890-8929 MeSH : D009379 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 tumor This oncology article is a stub .
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Pityriasis Rotunda
Wikipedia
External links [ edit ] Classification D DiseasesDB : 32814 External resources eMedicine : article/1107624 v t e Papulosquamous disorders Psoriasis Pustular Generalized pustular psoriasis ( Impetigo herpetiformis ) Acropustulosis / Pustulosis palmaris et plantaris ( Pustular bacterid ) Annular pustular psoriasis Localized pustular psoriasis Other Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis Parapsoriasis Pityriasis lichenoides ( Pityriasis lichenoides et varioliformis acuta , Pityriasis lichenoides chronica ) Lymphomatoid papulosis Small plaque parapsoriasis ( Digitate dermatosis , Xanthoerythrodermia perstans ) Large plaque parapsoriasis ( Retiform parapsoriasis ) Other pityriasis Pityriasis rosea Pityriasis rubra pilaris Pityriasis rotunda Pityriasis amiantacea Other lichenoid Lichen planus configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other: Hepatitis-associated lichen planus Lichen planus pemphigoides Other Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti–Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease This Genodermatoses article is a stub .
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Physiological Anisocoria
Wikipedia
It is generally considered to be benign, though it must be distinguished from Congenital Horner's syndrome , pharmacological dilatation or other conditions connected to the sympathetic nervous system . [1] The prevalence of physiological anisocoria has not been found to be influenced by the sex, age, or iris color of the subject.
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Leptospirosis
Orphanet
However, leptospirosis is often diagnosed late, due to its wide spectrum of symptoms, ranging from a flu-like syndrome to renal failure. Differential diagnosis The symptoms mimic the clinical presentations of many other diseases, including dengue fever and malaria.ACHE, ADA, BCHE, MAT1A, ACAT1, TLR2, IL1B, TNF, CXCL8, ANK1, HAP1, CCL2, SPTB, IL10, TLR1, CCL3, TCOF1, SELE, S100B, S100A1, REN, TLR4, SERPINA3, TTR, TYRP1, MME, SCRN1, CADM1, SUMF2, SLCO1B3, IL22, NOD2, WDR26, ELMOD3, LRG1, CST9, PHETA1, CLYBL, VDAC1, LAMB1, MICE, LGALS3, APEX1, APOA1, AZU1, CASP3, CD40LG, CES1, CISH, CRP, F10, FUT4, GEM, CXCR3, CXCL1, CXCL2, HLA-DQB1, HLA-DRB1, HP, HSPD1, ICAM1, IL6, CXCR2, IL12RB1, IL17A, IL18, ITGAM, KIR3DL1, LBP, SLCO1B7
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Scalp Dysesthesia
Wikipedia
Another theory is that people who have this condition (sometimes called "ponytail syndrome") have super-sensitive nerves in their scalp.