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Spinocerebellar ataxia type 23

ORPHA:101108· ICD-10 G11.2

Definition

Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.

Prevalence
<1 / 1 000 000
Inheritance
Autosomal dominant
Age of onset
Adult