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.

648
Articles
136
Trials (3 AU)
Updated
5 April 2026
Loading...

Common Questions

What is 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.

How many clinical trials are available for Spinocerebellar Ataxia?

RareWays currently indexes 136 clinical trials for Spinocerebellar Ataxia, of which 30 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Spinocerebellar Ataxia come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

Get research updates

Monthly email when new findings are published for Spinocerebellar Ataxia.

No spam. Unsubscribe any time. Not medical advice.

This information is for general awareness only.

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