98 top medical experts on Myoclonic Cerebellar Dyssynergia across 12 countries and 4 U.S. states, including 8 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 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)
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Spinocerebellar Degenerations (2,263).
  4. Synonyms: Cerebellar Dyssynergia,  Dentate Cerebellar Atrophy,  Dyssynergia Cerebellaris Myoclonica,  Ramsay Hunt Cerebellar Syndrome


  

        

                    


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