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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.