Spinocerebellar ataxia type 35 (Q101096): Difference between revisions
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Ataxia espinocerebelar tipo 35 é um subtipo de ataxia cerebelar autossômica dominante tipo 1 caracterizado por início na idade adulta de ataxia progressiva de marcha e de membros, disartria, dismetria ocular, tremor, hiperreflexia e torcicolo. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 35 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, tremor, hyperreflexia and torticollis. | |||
Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 35 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, tremor, hyperreflexia and torticollis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1674449075 |
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| English | Spinocerebellar ataxia type 35 |
Spinocerebellar ataxia type 35 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by the adult-onset of progressive gait and limb ataxia, dysarthria, ocular dysmetria, tremor, hyperreflexia and torticollis. |
