Spinocerebellar ataxia type 3 (Q101110): Difference between revisions
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Ataxia espinocerebelar tipo 3 (SCA3), também conhecida como Doença de Machado-Joseph, é o subtipo mais comum de ataxia cerebelar autossômica dominante tipo 1 (ACAD tipo 1), e que é caracterizada por ataxia, oftalomoplegia progressiva externa e outras manifestações neurológicas. | |||
| description / en | description / en | ||
Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is the most common subtype of type 1 autosomal dominant cerebellar ataxia (ADCA type 1), a neurodegenerative disorder, and is characterised by ataxia, external progressive ophthalmoplegia, and other neurological manifestations. | |||
Revision as of 17:54, 16 August 2026
Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is the most common subtype of type 1 autosomal dominant cerebellar ataxia (ADCA type 1), a neurodegenerative disorder, and is characterised by ataxia, external progressive ophthalmoplegia, and other neurological manifestations.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1991007405 |
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| English | Spinocerebellar ataxia type 3 |
Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is the most common subtype of type 1 autosomal dominant cerebellar ataxia (ADCA type 1), a neurodegenerative disorder, and is characterised by ataxia, external progressive ophthalmoplegia, and other neurological manifestations. |
