16 top medical experts on Spinocerebellar ataxia 26 across 1 countries and 2 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spinocerebellar ataxia 26: A very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: SCA26 Spinocerebellar ataxia 26,  Spinocerebellar ataxia type 26


  

        

                    


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