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Fibronectin Glomerulopathy
Orphanet
Clinical description Fibronectin glomerulopathy may present at different ages, although mostly in adolescence or early adulthood, with typical features of a nephrotic syndrome including hypertension, which can be severe, and edema, which initially develops around the eyes and legs but with time may become generalized.
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Acute Disseminated Encephalomyelitis
Orphanet
Differential diagnosis also includes infectious encephalitis, Guillain-Barré syndrome, glioblastoma multiforme, Schilder's disease (see these terms), psychotic disorders with acute onset, toxic/metabolic encephalopathy, vasculitis, nonvasculitic autoimmune encephalopathy, meningitis, metastatic tumor.
- Acute Hepatic Porphyria Orphanet
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Benign Paroxysmal Torticollis Of Infancy
Orphanet
Differential diagnosis The differential diagnosis (mainly in the first episode) should include intoxication, undesirable secondary effects of drugs, craniocervical junction abnormalities such as atlanto-axial instability, Arnold-Chiari malformation, epilepsy, vertigo, Sandifer's syndrome and posterior fossa tumors in cases with associated symptoms.
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Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii
Omim
Majewski (1992) gave a full account of a brother and sister and concluded that the facial appearance in this disorder is quite different from that of Seckel syndrome and very similar to that presented in a portrait reproduced as Figure 7 in Bondeson (1992).
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Nervous System Neoplasm
Wikipedia
Types include: Nerve sheath tumor Brain tumor Arachnoid cyst Optic nerve glioma References [ edit ] External links [ edit ] Classification D ICD - 10 : C69 - C72 D31 - D33 MeSH : D009423 v t e Overview of tumors , cancer and oncology Conditions Benign tumors Hyperplasia Cyst Pseudocyst Hamartoma Malignant progression Dysplasia Carcinoma in situ Cancer Metastasis Primary tumor Sentinel lymph node Topography Head and neck ( oral , nasopharyngeal ) Digestive system Respiratory system Bone Skin Blood Urogenital Nervous system Endocrine system Histology Carcinoma Sarcoma Blastoma Papilloma Adenoma Other Precancerous condition Paraneoplastic syndrome Staging / grading TNM Ann Arbor Prostate cancer staging Gleason grading system Dukes classification Carcinogenesis Cancer cell Carcinogen Tumor suppressor genes / oncogenes Clonally transmissible cancer Oncovirus Carcinogenic bacteria Misc.TP53, CDKN2A, ALK, MYCN, STAT6, NAB2, MDM2, APC2, LMO1, CHEK2, PHOX2B, SETD2, HACE1, NSD1, L2HGDH, LIN28B, TOP2A, NF2, RB1, NTRK1, PTN, VHL, TPM3, VEGFA, TXN, YEATS4, NEURL1, LZTR1, ENC1, LATS1, MVP, NXF1, GLIPR1, PART1, LNX1, NAV3, MIAT, NR2E1, RAB3A, SOX10, MDK, ATF1, BCHE, BRAF, CDKN2B, EGF, EPO, ERBB2, EWSR1, IDH1, IGFBP2, KIT, CD46, MGMT, CCL2, MSI1, MUTYH, MYC, NEU1, NF1, NGF, NGFR, POMC, PRL, PTEN, ASCL1, REST, LOC110806263
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Acral Fibrokeratoma
Wikipedia
ISBN 978-1-4160-2999-1 . 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 .
- Primary Hypomagnesemia With Secondary Hypocalcemia Orphanet
- Bleb (Medicine) Wikipedia
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Myoma
Wikipedia
External links [ edit ] Classification D ICD - 10 : D21 ICD - 9-CM : [1] ICD-O : M8895/3 MeSH : D009214 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 .
- Sterility (Physiology) Wikipedia
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Connective Tissue Neoplasm
Wikipedia
External links [ edit ] Classification D MeSH : D009372 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 v t e Tumours of bone and cartilage Diaphysis Multiple myeloma Epithelia Adamantinoma Primitive neuroectodermal tumor Ewing family Ewing's sarcoma Metaphysis Osteoblast Osteoid osteoma Osteoblastoma Osteoma / osteosarcoma Chondroblast Chondroma / ecchondroma / enchondroma Enchondromatosis Extraskeletal chondroma Chondrosarcoma Mesenchymal chondrosarcoma Myxoid chondrosarcoma Osteochondroma Osteochondromatosis Chondromyxoid fibroma Fibrous Ossifying fibroma Fibrosarcoma Epiphysis Chondroblast Chondroblastoma Myeloid Giant-cell tumor of bone Other Notochord Chordoma This article about a neoplasm is a stub .
- Mosaic Trisomy 8 Orphanet
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Perforated Eardrum
Wikipedia
External links [ edit ] Classification D ICD - 10 : H72 , S09.2 ICD - 9-CM : 384.2 MeSH : D018058 DiseasesDB : 13473 External resources MedlinePlus : 001038 eMedicine : ent/206 v t e Diseases of the outer and middle ear Outer ear Otitis externa Otomycosis Middle ear and mastoid Otitis media Mastoiditis Bezold's abscess Gradenigo's syndrome Tympanosclerosis Cholesteatoma Perforated eardrum Symptoms Ear pain Hearing loss Tests Otoscope pneumatic tympanometry v t e Nonmusculoskeletal injuries of head ( head injury ) and neck Intracranial see neurotrauma Extracranial/ facial trauma eye : Black eye Eye injury Corneal abrasion ear : Perforated eardrum Either/both Penetrating head injury
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Hypertrophic Scar
Wikipedia
Hypertrophic scars usually improve over one or two years, but may cause distress due to their appearance or the intensity of the itching; they can also restrict movement if they are located close to a joint. [ citation needed ] [ dubious – discuss ] Some people have an inherited tendency to hypertrophic scarring, for example, those with Ehlers–Danlos syndrome . Prevention and treatment [ edit ] It is not possible to completely prevent hypertrophic scars, so those with a history of them should inform their doctor or surgeon if they need surgery.TGFB1, CCN2, SMAD2, MIR21, SMN2, SMN1, DCN, SMAD3, IGF1, IL10, SMAD7, MMRN1, IL6, ACTB, TNF, PTN, AKT1, MMP2, PTEN, NREP, ELN, EGF, MIR145, HIF1A, TGFB3, PIK3CA, TP53, COL1A1, IFNG, FN1, TGFB1I1, COL18A1, TGFBR1, MC1R, ZEB2, MMP1, MMP9, MSC, SFRP2, SERPINE1, CXCL12, S100A12, PIK3CB, PIK3CD, PIK3CG, PPARG, CXCL8, TIMP1, CYLD, IL1B, COL3A1, COL1A2-AS1, GDF9, MIR98, ANXA5, FGF2, BCL2, BECN1, TP63, TRADD, MIR31, MIR29A, CXCR4, NR1I2, MIR222, MIR22, GEMIN2, PTPN5, VIM, MIR205, VEGFA, UVRAG, MIR495, MIR519D, MIR486-1, TRPC3, TPM3, MIR564, MIR663A, PGR-AS1, TNFAIP6, MIR6836, MIR494, SLC33A1, SCAF11, CSAD, PWAR1, LAMA1, MAP1LC3A, SLC25A32, MIR10A, SLC52A2, FKBP10, TIMP2, DIABLO, SLC52A1, WNT4, GHRL, SIRT7, BRD4, MIR200B, MIR130A, MIR137, SIRT1, MIR143, MIR155, MIR181C, MIR185, CKAP4, POSTN, MIR188, COX5A, SLC9A3R2, MIR192, SLC12A9, PTGS2, THBS4, HAS1, MARK2, F2R, F2RL1, FBP1, FGF13, CXCR3, HMGB1, CXCL10, HOXB9, IFNA1, IFNA13, IGFBP3, IL4, IL15, EDN1, CPOX, COX8A, CDKN3, CDKN1A, CD1A, CASP3, CALCA, DDR1, BMP7, CCND1, ATM, ARG1, AGTR2, AGTR1, AGT, ADRB3, IL17A, ITGA5, TGFBR2, RAG2, OSM, PCNA, PLAU, POMC, ADRB2, PTK2, RPE65, ITGB1, S100A8, CCL13, CX3CL1, TAT, ZEB1, TGFBI, NOS3, COX2, MSH3, ABCC1, MMP19, MMP13, MMP12, MDM4, SMAD4, LUM, LTBP3, LTBP2, LOX, KRT14, KRT10, EIF6, ITGB2, MTCO2P12
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Superinfection
Wikipedia
. ^ "Treatment of neutropenic fever syndromes in adults with hematologic malignancies and hematopoietic cell transplant recipients (high-risk patients)" . www.uptodate.com .ERVK-32, ERVK-18, ERVK-20, ERVW-1, IL10, CXCR4, HLA-B, CR2, HLA-C, IL1B, ITIH4, IFNA13, MYOM2, CCR5, NLRP3, IFNA1, PDHX, PDLIM7, NR1I3, TRIM13, TNF, CTCF, TMED2, TFRC, TPPP, SPG7, CCL2, CHP1, ACTB, DDX58, PLAAT4, AD12, CXADRP1, ACOT1, LINC01194, VHLL, NRSN1, PRRT2, IL33, PAGR1, ROBO3, CENPK, APOBEC3G, CPVL, IL23A, IL22, RPS23, PDGFB, PRKCB, GPT, GAST, FLT3LG, FCER2, ELANE, CXADR, CD74, CD9, CD4, CAT, CASR, CASP1, C1QBP, BCL6, BCL2, ARR3, GALNS, HDAC1, PRKCA, HLA-A, PRKAR1A, SLC25A3, ALB, NM, MMP8, LTB, PDX1, ING1, IL17A, CXCL8, IL6, IL1A, IFNAR2, TNC, HLA-DRB1, H3P19
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Haverhill Fever
Wikipedia
External links [ edit ] Classification D ICD - 10 : A25.1 ( ILDS A25.110) ICD - 9-CM : 026.1 MeSH : D011906 DiseasesDB : 30717 v t e Bacterial diseases due to gram negative non- proteobacteria ( BV4 ) Spirochaete Spirochaetaceae Treponema Treponema pallidum Syphilis / bejel Yaws Treponema carateum ( Pinta ) Treponema denticola Borrelia Borrelia burgdorferi / Borrelia afzelii Lyme disease Erythema migrans Neuroborreliosis Borrelia recurrentis ( Louse borne relapsing fever ) Borrelia hermsii / Borrelia duttoni / Borrelia parkeri ( Tick borne relapsing fever ) Leptospiraceae Leptospira Leptospira interrogans ( Leptospirosis ) Chlamydiaceae Chlamydia Chlamydia psittaci ( Psittacosis ) Chlamydia pneumoniae Chlamydia trachomatis Chlamydia Lymphogranuloma venereum Trachoma Bacteroidetes Bacteroides fragilis Tannerella forsythia Capnocytophaga canimorsus Porphyromonas gingivalis Prevotella intermedia Fusobacteria Fusobacterium necrophorum ( Lemierre's syndrome ) Fusobacterium nucleatum Fusobacterium polymorphum Streptobacillus moniliformis ( Rat-bite fever / Haverhill fever ) This infectious disease article is a stub .
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Protoporphyria, Erythropoietic, 2
Omim
Her father and paternal uncle had mild photosensitivity and accumulation of PPIX, but without the complete clinical syndrome of EPP. Inheritance The transmission pattern of EPP2 in the family reported by Yien et al. (2017) was consistent with autosomal dominant inheritance with variable expressivity.
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Lipoblastoma
Wikipedia
Retrieved 11 March 2011 . 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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Cavitary Pneumonia
Wikipedia
These alveoli can become enlarged by a number of processes: bacterial infection ( tuberculosis ), fungal infection, vasculitis ( granulomatosis with polyangiitis ), collagen vascular disease ( Sjögren's syndrome ) or granulomatous disease ( sarcoidosis ).