340 top medical experts on Spinocerebellar Degenerations across 48 countries and 24 U.S. states, including 159 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Spinocerebellar Degenerations: A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Cerebellar Diseases (1,413), Nervous System Heredodegenerative Disorders (865), Spinal Cord Diseases (2,625) and Narrower Categories: Friedreich Ataxia (828), Myoclonic Cerebellar Dyssynergia (98), Olivopontocerebellar Atrophies (610), Spinocerebellar Ataxias (1,752).
  4. Clinical Trials ClinicalTrials.gov : at least 82 including 8 Active, 40 Completed, 17 Recruiting
  5. Synonyms: Hereditary Ataxias,  Early Onset Cerebellar Ataxia,  Late Onset Cerebellar Ataxia,  Primary Cerebellar Degenerations,  Corticostriatal-Spinal Degeneration,  Marie Cerebellar Ataxia,  Marinesco-Sjogren Syndrome,  Spinocerebellar Degeneration


  

        

                    


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