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Spinocerebellar ataxia type 41
rareSpinocerebellar ataxia type 41 is a rare autosomal dominant cerebellar ataxia type III disorder characterized by adult-onset progressive imbalance and loss of coordination associated with an ataxic gait. Mild atrophy of the cerebellar vermis has been reported on brain magnetic resonance imaging.
- Identifiers
- MONDO:0014626 OMIM:616410Orphanet:458798
- Causal genes
- TRPC3
- Also known as
- SCA41 · spinocerebellar ataxia 41
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