Spinocerebellar ataxia type 7 (Q101071): Difference between revisions
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Ataxia espinocerebelar tipo 7 (SCA7) é um transtorno autossômico dominante que envolve ataxia progressiva, disartria, disfagia, bem como perda de visão central devida a distrofia retiniana cone-bastonete. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disorder that involves progressive ataxia, dysarthria, dysphagia, as well as central vision loss due to cone-rod retinal dystrophy. | |||
Revision as of 17:52, 16 August 2026
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disorder that involves progressive ataxia, dysarthria, dysphagia, as well as central vision loss due to cone-rod retinal dystrophy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_625800545 |
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| English | Spinocerebellar ataxia type 7 |
Spinocerebellar ataxia type 7 (SCA7) is an autosomal dominant disorder that involves progressive ataxia, dysarthria, dysphagia, as well as central vision loss due to cone-rod retinal dystrophy. |
