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atrofie olivopontocerebelárne

  1. Subject h.atrofie olivopontocerebelárne
    Subject h.Olivopontocerebellar Atrophies
    Entry termsatrofia olivopontocereberálna
    Déjerineov-Thomasov syndróm
    Déjerine-Thomasov syndróm
    atrofia olivopontocereberálna familiárna
    atrofia olivopontocereberálna vrodená
    atrofia olivopontocereberálna hereditárna
    atrofia olivopontocerebelárna nefamiliárna
    atrofia olivopontocereberálna idiopatická
    atrofia olivo-ponto-cereberálna
    degenerácia olivo-ponto-cerebelárna
    degenerácia olivopontocerebelárna
    atrofia olivopontocerebelárna
    hypoplázia olivopontocerebelárna
    atrofia pontoolivocerebelárna
    ataxia presenilná
    English X referencesDejerine-Thomas Syndrome
    Olivopontocerebellar Atrophy, Idiopathic
    Olivopontocerebellar Hypoplasia
    Scope note in EnglishA group of inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary nuclei. Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA. The familial form has an earlier onset (second decade) and may feature spinal cord atrophy. The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)
    See also reference (FX) in Slovak degenerácia olivárna
    See also reference (FX) in English Olivary Degeneration
    Links (1) - ARTICLES
    (2) - MeSH descriptor
    (2) - BOOKS
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Number of the records: 1  

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