Spinocerebellar ataxia type 3 (Q101110): Difference between revisions

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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.
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    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.

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