Spinocerebellar ataxia type 32

What is Spinocerebellar ataxia type 32?

An autosomal dominant cerebellar ataxia type 1 that is characterized by ataxia and cognitive impairment. Azoospermia is a typical feature in affected males.

Other condition names

  • Cerebellar ataxia with azoospermia and intellectual disability
  • SCA32

Inheritance type

Autosomal dominant


  • Worldwide: <1 in 1,000 000

Age of Onset

  • Adult
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.