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Spinocerebellar ataxia type 23

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Name:
Spinocerebellar ataxia type 23
Description:
Spinocerebellar ataxia type 23 (SCA23) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by gait ataxia, dysarthria, slowed saccades, ocular dysmetria, Babinski sign and hyperreflexia.
ORPHAcode:
101108
Synonyms:
SCA23
XREF(s):
Orphanet
OMIM
ICD-10
MeSH
Analyte(s):
PDYN
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14