73 top medical experts on Spinocerebellar ataxia 13 across 4 countries and 6 U.S. states, including 15 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spinocerebellar ataxia 13: Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.
  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: Autosomal dominant cerebellar ataxia with mental retardation,  autosomal dominant with mental retardation Cerebellar ataxia,  SCA13 Spinocerebellar ataxia 13


  

        

                    


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