Spinocerebellar ataxia type 32 (SCA32)

Evidence-based neurology checklist on spinocerebellar ataxia type 32 (sca32): Genetics This is caused by mutations in chromosome 7q The transmission is autosomal dominant Clinical features Magnetic resonance imaging (MRI) brain Information on source

Genetics

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

Clinical features

Magnetic resonance imaging (MRI) brain

Information on source

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...