Spinocerebellar ataxia type 25 (SCA25)

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

Spinocerebellar ataxia type 25 (SCA25). This is caused by mutations in chromosome 2p. Fully referenced neurology checklist.

Genetics

  • This is caused by mutations in chromosome 2p
  • The transmission is autosomal dominant
  • The onset age is 1-39 years

Clinical features

Locked: subscribe to see this section.

Differential diagnosis

Locked: subscribe to see this section.

Investigations

Locked: subscribe to see this section.

References

  1. Stevanin G, Bouslam N, Thobois S, et al. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Ann Neurol 2004; 55:97-104.
  2. Whaley NR, Fujioka S, Wszolek ZK. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics. Orphanet J Rare Dis 2011; 6:33.
  3. Stevanin G, Broussolle E, Streichenberger N, Kopp N, Brice A, Durr A. Spinocerebellar ataxia with sensory neuropathy (SCA25). Cerebellum 2005; 4:58-61.

Related checklists

Loading...