Spinocerebellar ataxia type 10 (Q101074): Difference between revisions

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Latest revision as of 17:52, 16 August 2026

Spinocerebellar ataxia type 10 (SCA10) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances. The most common type of epilepsy is generalised motor seizures, but partial motor or partial complex seizures can occur.

Language	Label	Description	Also known as
default for all languages	ID_157300879
English	Spinocerebellar ataxia type 10	Spinocerebellar ataxia type 10 (SCA10) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances. The most common type of epilepsy is generalised motor seizures, but partial motor or partial complex seizures can occur.