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atrofie spinálne svalové, infantilný a juvenilný typ

  1. Subject h.atrofie spinálne svalové, infantilný a juvenilný typ
    Subject h.Spinal Muscular Atrophies of Childhood
    Entry termsatrofie spinálne svalové detské
    atrofie spinálne svalové, v detstve
    atrofia spinálna muskulárna, infantilný typ
    atrofia spinálna muskulárna, juvenilný typ
    Werdnigova-Hoffmannova choroba
    atrophia spinalis progressiva infantilis
    HMN proximálny typ I
    atrofia svalová spinálna detská
    Kugelbergova-Welanderovej choroba
    atrofia spinálna svalová juvenilná
    English X referencesInfantile Spinal Muscular Atrophy
    Juvenile Spinal Muscular Atrophy
    Kugelberg-Welander Disease
    Muscular Atrophy, Spinal, Infantile
    Spinal Muscular Atrophy, Infantile
    Spinal Muscular Atrophy, Juvenile
    Werdnig-Hoffmann Disease
    Scope note in EnglishA group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3)
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    (2) - CiBaMed
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