Spinocerebellar ataxia type 41 (SCA41)

Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .

Spinocerebellar ataxia type 41 (SCA41). This is likely caused by mutations in the TRPC3 gene on chromosome 4q. Fully referenced neurology checklist.

Genetics

  • This is likely caused by mutations in the TRPC3 gene on chromosome 4q
  • The transmission is autosomal dominant

Clinical features

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Investigations

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References

  1. Fogel BL, Hanson SM, Becker EB. Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans? Mov Disord 2015; 30:284-286.
  2. Becker EB, Fogel BL, Rajakulendran S, et al. Candidate screening of the TRPC3 gene in cerebellar ataxia. Cerebellum 2011; 10:296-299.

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