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Spinocerebellar ataxia type 26

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Name:
Spinocerebellar ataxia type 26
Description:
A very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III) characterized by late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities.
ORPHAcode:
101112
Synonyms:
SCA26
XREF(s):
Orphanet
MeSH
ICD-10
OMIM
Analyte(s):
EEF2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14