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Spinocerebellar ataxia type 17
rareA rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.
- Causal genes
- TBP
- Part of
- Huntington disease-like syndromeAutosomal dominant cerebellar ataxia type ICerebelloparenchymal disorder
- Also known as
- cerebelloparenchymal disorder II · CPD2 · HDL4 · Huntington disease-like 4 · olivopontocerebellar atrophy 5
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