Spinocerebellar ataxia type 32 (SCA32)

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

Spinocerebellar ataxia type 32 (SCA32). This is caused by mutations in chromosome 7q. Fully referenced neurology checklist.

Genetics

  • This is caused by mutations in chromosome 7q
  • The transmission is autosomal dominant

Clinical features

Locked: subscribe to see this section.

Magnetic resonance imaging (MRI) brain

Locked: subscribe to see this section.

Information on source

Locked: subscribe to see this section.

References

  1. Jiang H, Zhu H-P, Gomez CM. SCA32: an autosomal dominant cerebellar ataxia with azoospermia maps to chromosome 7q32-q33. (Abstract) Mov Disord 2010; 25: S192.

Related checklists

Loading...