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Spinocerebellar ataxia type 13

rare

Spinocerebellar ataxia type 13 (SCA13) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by onset in childhood marked by delayed motor and cognitive development followed by mild progression of cerebellar ataxia.

Identifiers
MONDO:0011529 OMIM:605259Orphanet:98768
Causal genes
KCNC3
Part of
Autosomal dominant cerebellar ataxia type I
Also known as
autosomal dominant cerebellar ataxia with intellectual disability · autosomal dominant cerebellar ataxia with mental retardation · cerebellar ataxia, autosomal dominant with intellectual disability · cerebellar ataxia, autosomal dominant with mental retardation · SCA13

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