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Autosomal dominant cerebellar ataxia type III

Autosomal dominant cerebellar ataxia (ACDA) type III is a group of neurodegenerative disorders characterized by mostly pure cerebellar syndromes with occasional non-cerebellar signs (e.g. pyramidal signs, peripheral neuropathy, writer's cramp) and includes spinocerebellar ataxia (SCA) type 5 (SCA5), SCA6, SCA11, SCA26, SCA30, and SCA31.

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Spinocerebellar ataxia type 6 9 trials
Spinocerebellar ataxia 45 0 trials
Spinocerebellar ataxia type 11 0 trials
Spinocerebellar ataxia type 26 0 trials
Spinocerebellar ataxia type 30 0 trials
Spinocerebellar ataxia type 31 0 trials
Spinocerebellar ataxia type 38 0 trials
Spinocerebellar ataxia type 41 0 trials
Spinocerebellar ataxia type 42 0 trials Sub-types →
Spinocerebellar ataxia type 5 0 trials