Spinocerebellar ataxia type 13 (Q101088): Difference between revisions
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Ataxia espinocerebelar tipo 13 (SCA13) é um subtipo muito raro de ataxia cerebeçar autossômica dominante tipo 1 (ACAD tipo I). É caracterizada por início na infância marcado por atraso do desenvolvimento psicomotor seguido por progressão leve de ataxia cerebelar. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia. | |||
Revision as of 17:53, 16 August 2026
Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1191033828 |
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| English | Spinocerebellar ataxia type 13 |
Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia. |
