fibrodysplasia
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Fibrodysplasia — may refer to:* Fibrodysplasia ossificans progressiva, a rare disease in which fibrous tissue such as muscle turns to bone when damaged. * Fibromuscular dysplasia, a disease characterized by the fibrous thickening of the renal artery. * Fibrous… … Wikipedia
Fibrodysplasia ossificans progressiva — Infobox Disease Name = Fibrodysplasia ossificans progressiva Caption = DiseasesDB = 8732 ICD10 = ICD10|M|61|1|m|60 ICD9 = ICD9|728.11 ICDO = OMIM = 135100 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 609 MeshID = D009221 Fibrodysplasia… … Wikipedia
Fibrodysplasia ossificans progressiva — Klassifikation nach ICD 10 M61.1 Myositis ossificans progressiva Fibrodysplasia ossificans progressiva … Deutsch Wikipedia
Fibrodysplasia Ossificans Progressiva — Klassifikation nach ICD 10 M61.1 Myositis ossificans progressiva Fibrodysplasia ossificans progressiva … Deutsch Wikipedia
Fibrodysplasia ossificans muliplex progressiva — Klassifikation nach ICD 10 M61.1 Myositis ossificans progressiva Fibrodysplasia ossificans progressiva … Deutsch Wikipedia
fibrodysplasia — Abnormal development of fibrous connective tissue. f. ossificans progressiva [MIM*135100] a generalized disorder of connective tissue in which there is ectopic ossification with bone replacing tendons, fasciae, and ligaments; a lethal … Medical dictionary
fibrodysplasia — n. abnormal development affecting connective tissue … The new mediacal dictionary
fibrodysplasia ossificans progressiva — noun A very rare disease of the connective tissue in which fibrous tissue (including muscle, tendon, and ligament) becomes ossified when damaged … Wiktionary
Fibrodysplasia ossificans progressiva (FOP) — A rare but dramatic genetic disorder that turns muscles, tendons and ligaments into bone, threatening to transform the victim into a statue of stone. FOP is characterized by physical handicap due to bone forming in the wrong places and malformed… … Medical dictionary
fibrodysplasia ossificans progressiva — a rare, progressive, fatal, autosomal dominant disorder caused by mutation of the ACVR1 gene (locus: 2q23 q24), which encodes a receptor that signals a specific transcriptional response related to growth and differentiation. It is characterized… … Medical dictionary
