Spinocerebellar ataxia type 11 (Q101081): Difference between revisions
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Ataxia espinocerebelar tipo 11 é um subtipo de ataxia cerebelar autossômica dominante tipo 3, caracterizada por início precoce de sinais cerebelares, anormalidades do movimento ocular e sinais piramidais, e que é causado por mutação no gene TTBK2. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 11 is a subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs and caused by a mutation in the TTBK2 gene. | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 11 is a subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs and caused by a mutation in the TTBK2 gene.
| Language | Label | Description | Also known as |
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| default for all languages | ID_743674840 |
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| English | Spinocerebellar ataxia type 11 |
Spinocerebellar ataxia type 11 is a subtype of autosomal dominant cerebellar ataxia type 3, characterised by the early onset of cerebellar signs, eye movement abnormalities and pyramidal signs and caused by a mutation in the TTBK2 gene. |
