ICD G11.1ORPHA:99SCA

Spinocerebellar Ataxia

Spinocerebellar Ataxia refers to a group of inherited progressive neurological disorders characterised by degeneration of the cerebellum and its connections, causing difficulty walking, poor coordination, and speech problems. More than 40 genetic subtypes have been identified. There is currently no disease-modifying treatment, but active clinical trials are under way.

675
Articles
3078
Trials (90 AU)
Updated
5 April 2026
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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.