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Spinocerebellar ataxia type 45

ORPHA:589527· ICD-10 G11.8

Definition

A rare autosomal dominant cerebellar ataxia characterized by slowly progressive late-onset gait and limb ataxia, dysarthria, and variable nystagmus. Brain imaging reveals cerebellar atrophy.

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