Autosomal dominant cerebellar ataxia type 3 (Q85241): Difference between revisions

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Latest revision as of 10:36, 15 August 2026

Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.

Language	Label	Description	Also known as
default for all languages	ID_390406504
English	Autosomal dominant cerebellar ataxia type 3	Group of autosomal dominant cerebellar ataxias referred to as spinocerebellar ataxias (SCAs) that are characterized by dysarthria, variable reflexes, extrapyramidal rigidity, dystonia, bulbar signs, distal motor weakness, polyneuropathy, or ophthalmoplegia. Several are associated with coding CAG repeat expansions and display genetic anticipation across generations.