Spinocerebellar ataxia type 10 (Q101074): Difference between revisions
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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.
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| default for all languages | ID_157300879 |
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| 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. |
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CID11:ID_157300879
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