Spinocerebellar ataxia type 6 (Q101078): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Ataxia espinocerebelar tipo 6 (SCA6) é um subtipo comum de ataxia cerebelar autossômica dominante tipo 3, mais usualmente observado em Japão, Coreia, Países Baixos e Alemanha, caracterizada por início tardio e ataxia de marcha lentamente progressiva, sinais cerebelares e problemas de movimentação ocular, e causada por mutação no gene CACNA1A. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene. | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1056119281 |
||
| English | Spinocerebellar ataxia type 6 |
Spinocerebellar ataxia type 6 is a common subtype of autosomal dominant cerebellar ataxia type 3, most commonly seen in Japan, Korea, the Netherlands and Germany, characterised by late-onset and slowly progressive gait ataxia, cerebellar signs and eye movement problems and caused by mutations in the CACNA1A gene. |
