68 top medical experts on Spinocerebellar Ataxia 29 across 8 countries and 2 U.S. states, including 10 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spinocerebellar Ataxia 29: An autosomal dominant cerebellar ataxia type I that is characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

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  • Synonyms: Aplasia of cerebellar vermis,  autosomal dominant nonprogressive congenital Cerebellar ataxia,  nonprogressive early-onset Cerebellar ataxia,  Cerebellar vermis aplasia,  SCA29 Spinocerebellar Ataxia 29


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