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Spinocerebellar ataxia type 35
What is Spinocerebellar ataxia type 35?
An autosomal dominant cerebellar ataxia type 1 that is characterized by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, intention tremor of hands, hyperreflexia and spasmodic torticollis.
Other condition names
SCA35
Inheritance type
Autosomal dominant
Prevalence
Worldwide: <1 in 1,000 000
Age of Onset
Adolescent
Adult
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.