Spinocerebellar ataxia type 23 (Q101095): Difference between revisions
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Ataxia espinocerebelar tipo 23 (SCA23) é um subtipo muito raro de ataxia cerebeçar autossômica dominante tipo 1 (ACAD tipo I). É caracterizada por ataxia de marcha, disartria, sácades lentas, dismetria ocular, sinal de Babinski e hiperreflexia. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia. | |||
Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1340267869 |
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| English | Spinocerebellar ataxia type 23 |
Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia. |
