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Dyssynergia cerebellaris myoclonica

Introduction: Dyssynergia cerebellaris myoclonica

Description of Dyssynergia cerebellaris myoclonica

Dyssynergia cerebellaris myoclonica: 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)
Source: Diseases Database

Dyssynergia cerebellaris myoclonica: Related Topics

These medical condition or symptom topics may be relevant to medical information for Dyssynergia cerebellaris myoclonica:

Terms associated with Dyssynergia cerebellaris myoclonica:

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Source: Diseases Database

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