Spinocerebellar ataxia type 36 (Q101105): Difference between revisions
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Ataxia espinocerebelar tipo 36 é um subtipo de ataxia cerebelar autossômica dominante tipo 1 caracterizado por ataxia de marcha e de membros, espasticidade de membros inferiores, disartria, fasciculações musculares, atrofia de língua e hiperreflexia. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasciculations, tongue atrophy and hyperreflexia. | |||
Revision as of 17:54, 16 August 2026
Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasciculations, tongue atrophy and hyperreflexia.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1544814018 |
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| English | Spinocerebellar ataxia type 36 |
Spinocerebellar ataxia type 36 is a subtype of autosomal dominant cerebellar ataxia type 1 characterised by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasciculations, tongue atrophy and hyperreflexia. |
