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Up to: Huntington disease-like syndrome · Autosomal dominant cerebellar ataxia type I
Machado-Joseph disease
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 characterized by ataxia, external progressive ophthalmoplegia, and other neurological manifestations.
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Machado-Joseph disease type 3 2 trials
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Machado-Joseph disease type 1 0 trials
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Machado-Joseph disease type 2 0 trials
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Machado-Joseph disease type 4 0 trials