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GENATLAS PHENOTYPE

last update : 02-12-2022

Symbol	SCAR32
Location	10q26.11
Name	spinocerebellar ataxia, autosomal recessive 32
Corresponding gene	PRDX3
Main clinical features	onset of gait ataxia in the second or third decades of life, slowly progressive including upper limb ataxia, oculomotor signs, dysphagia, and dysarthria also hyper- or hypokinetic movement abnormalities brain imaging shows cerebellar atrophy
Genetic determination	autosomal recessive
Function/system disorder	neurology
Type	disease

Remark(s)