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GENATLAS PHENOTYPE

last update : 27-08-2014

Symbol	SCA26
Location	19p13.3
HGNC id	31097
Name	spinocerebellar ataxia 26
Corresponding gene	EEF2
Main clinical features	pure, with slowly progressive gait ataxia, upper limb ataxia, and dysarthria, on MRI, atrophy of the cerebellum sparing the pons and medulla
Genetic determination	autosomal dominant
Function/system disorder	neurology
Type	disease

Remark(s)

adjacent to SCA6