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Spinocerebellar ataxia type 36

What is Spinocerebellar ataxia type 36?

An autosomal dominant cerebellar ataxia type 1 that characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia.

Other condition names

  • Asidan
  • SCA36

Inheritance type

Autosomal dominant

Prevalence

  • Worldwide: Unknown

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.