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Dictionary » Myoclonic Cerebellar Dyssynergia
 

Myoclonic Cerebellar Dyssynergia

Introduction: Myoclonic Cerebellar Dyssynergia

Description of Myoclonic Cerebellar Dyssynergia

Myoclonic Cerebellar Dyssynergia: 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: MeSH 2007

Myoclonic Cerebellar Dyssynergia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Myoclonic Cerebellar Dyssynergia:

Terms associated with Myoclonic Cerebellar Dyssynergia:

Terms Similar to Myoclonic Cerebellar Dyssynergia:

Source - MeSH 2007

Broader terms for Myoclonic Cerebellar Dyssynergia

Source - MeSH 2007

Hierarchical classifications of Myoclonic Cerebellar Dyssynergia

The following list attempts to classify Myoclonic Cerebellar Dyssynergia into categories where each line is subset of the next.

MeSH 2007 Hierarchy:

MeSH 2007 Hierarchy

MeSH 2007 Hierarchy

MeSH 2007 Hierarchy

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