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Ataxia-oculomotor apraxia type 1

ORPHA:1168· ICD-10 G11.3

Definition

A rare autosomal recessive cerebellar ataxia, characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.

Prevalence
Unknown
Inheritance
Autosomal recessive
Age of onset
Childhood