Spinocerebellar ataxia type 3 (Q101110)
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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 |
|---|---|---|---|
| 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. |
Statements
CID11:ID_1991007405
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