Spinocerebellar ataxia type 10 (Q101074): Difference between revisions
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Ataxia espinocerebelar tipo 10 (SCA10) é um subtipo de ataxia cerebelar autossômico dominante tipo 1 (ACAD tipo I). É caracterizada por síndrome cerebelar lentamente progressiva e epilepsia, algumas vezes com sinais piramidais leves, neuropatia periférica e distúrbios neuropsicológicos. O tipo mais comum de epilepsia são crises motoras generalizadas, mas convulsões parciais motoras ou convulsões parciais complexas podem ocorrer. | |||
| description / en | description / en | ||
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. | |||
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 |
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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. |
