Spinocerebellar ataxia type 20

MONDO:0012098

Spinocerebellar ataxia type 20 (SCA20) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by cerebellar dysarthria as the initial typical manifestation.

Also known as: SCA20, spinocerebellar ataxia type 20, chromosome 11q12 duplication syndrome, 260-Kb, spinocerebellar ataxia 20, spinocerebellar ataxia with dysphonia, spinocerebellar ataxia with spasmodic cough

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 20 itself.

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↑ Autosomal dominant cerebellar ataxia type I (16)

Including sub-types (19) Tagged with Spinocerebellar ataxia type 20 (0)

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