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Spinocerebellar ataxia type 6

ORPHA:98758· ICD-10 G11.2

Definition

An autosomal dominant cerebellar ataxia type III that is characterized by late-onset and slowly progressive gait ataxia and other cerebellar signs such as impaired muscle coordination and nystagmus.

Prevalence
1-9 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Adolescent, Adult, Elderly