Spinocerebellar ataxia type 4 (Q101101): Difference between revisions
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Ataxia espinocerebelar tipo 4 (SCA4) é um subtipo muito raro, progressivo e intratável de ataxia cerebelar autossômica dominante (ACAD tipo I) caracterizado por ataxia com neuropatia sensitiva. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy. | |||
Revision as of 17:54, 16 August 2026
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1686006145 |
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| English | Spinocerebellar ataxia type 4 |
Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterised by ataxia with sensory neuropathy. |
