Spinocerebellar ataxia- autosomal recessive 3
Overview
Spinocerebellar ataxia, autosomal recessive 3: A rare neurological disorder caused by a genetic defect (chromosome 6p21, recessive) and resulting in ataxia and loss of vision and hearing.
Symptoms
* Hearing loss * Vision loss * Ataxia
Causes
* Ataxia * Hearing loss * Vision loss