Autosomal dominant cerebellar ataxia type 4 (Q85247): Difference between revisions

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Latest revision as of 10:36, 15 August 2026

Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus.

Language	Label	Description	Also known as
default for all languages	ID_745970501
English	Autosomal dominant cerebellar ataxia type 4	Autosomal dominant cerebellar movement disorder characterized by ataxia, atrophy, unsteady gait, dysarthria, and distinct peripheral neuropathy. Typically begins in the fourth or fifth decade of life, with continued progression of symptoms. Considered a Type III ADCA that is associated with a mutation at the 16q22 gene locus.