7 top medical experts on autosomal recessive 6 Spinocerebellar ataxia across 2 countries and 1 U.S. states. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. autosomal recessive 6 Spinocerebellar ataxia: A rare, genetic, autosomal recessive cerebellar ataxia disease characterized by nonprogressive cerebellar ataxia, with onset in infancy, manifesting with delayed motor and speech development, gait ataxia, dysmetria, hypotonia, increased deep tendon reflexes, and dysarthria. Additional variable manifestations include moderate nystagmus on lateral gaze, mild spasticity, intention tremor, short stature and pes planus. Brain imaging reveals cerebellar vermis atrophy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: autosomal recessive infantile nonprogressive Cerebellar ataxia,  Norwegian infantile onset ataxia


  

        

                    


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