DYSSYNERGIA CEREBELLARIS MYOCLONICA
\dˈɪsɪnəd͡ʒə sˈɛɹɪbˌɛlɑːɹˌɪs mˌa͡ɪəklˈɒnɪkə], \dˈɪsɪnədʒə sˈɛɹɪbˌɛlɑːɹˌɪs mˌaɪəklˈɒnɪkə], \d_ˈɪ_s_ɪ_n_ə_dʒ_ə s_ˈɛ_ɹ_ɪ_b_ˌɛ_l_ɑː_ɹ_ˌɪ_s m_ˌaɪ_ə_k_l_ˈɒ_n_ɪ_k_ə]\
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A 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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Nearby Words
- dyssomnias
- dysspermatism
- dysspermatism, dysspermia
- dyssyllabia
- dyssynergia
- Dyssynergia Cerebellaris Myoclonica
- dyssynergia cerebellaris progressiva
- dyssynergia cerehellaris progressiva
- dyssynodus
- dyssynusia
- dyssystole