Spinocerebellar ataxia type 17 (Q101090): Difference between revisions
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Ataxia espinocerebelar tipo 17 (SCA17) é um subtipo raro de ataxia cerebeçar autossômica dominante tipo 1 (ACAD tipo I). É caracterizada por um quadro clínico variável que pode incluir demência, transtornos psiquiátricos, parkinsonismo, distonia, coreia, espasticidade e epilepsia. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 17 (SCA17) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy. | |||
Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 17 (SCA17) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1173627424 |
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| English | Spinocerebellar ataxia type 17 |
Spinocerebellar ataxia type 17 (SCA17) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy. |
