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dyssynergia mozočka myoklonická

  1. Subject h.dyssynergia mozočka myoklonická
    Subject h.Myoclonic Cerebellar Dyssynergia
    Entry termsdyssynergia mozočka
    atrofia ozubeného jadra mozočka
    nucleus dentatus, atrofia
    dyssynergia cerebellaris myoclonica
    Ramsay Huntov mozočkový syndróm
    English X referencesCerebellar Dyssynergia
    Dentate Cerebellar Atrophy
    Dyssynergia Cerebellaris Myoclonica
    Ramsay Hunt Cerebellar Syndrome
    Scope note in EnglishA condition marked by progressive CEREBELLAR ATAXIA combined with MYOCLONUS usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal SEIZURES, spasticity, and DYSKINESIAS. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the CEREBELLUM are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1)
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