Spinocerebellar ataxia type 22 (Q101080): 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 22 (SCA22) é um subtipo muito raro de ataxia cerebeçar autossômica dominante tipo 1 (ACAD tipo I). É caracterizado por ataxia cerebelar de progressão lenta e hiporreflexia. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 22 (SCA22) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar ataxia and hyporeflexia. | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 22 (SCA22) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar ataxia and hyporeflexia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1835077432 |
||
| English | Spinocerebellar ataxia type 22 |
Spinocerebellar ataxia type 22 (SCA22) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterised by slowly progressive cerebellar ataxia and hyporeflexia. |
