Spinocerebellar ataxia 4
Other Names for this Disease
- Spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy
- Spinocerebellar ataxia type 4
On this page
- The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.
The Ataxia Patient Registry at CoRDS was established to facilitate the establishment of rare disease registries for all rare diseases with a specific questionnaire for those with any type of ataxia or those at risk for ataxia.