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Medical Term:

ataxia with infantile onset olivopontocerebellar atrophy

 

Definition: an autosomal recessive multisystem disease of infantile onset, manifesting ataxia, polyneuropathy, dysarthria, deafness, seizures, and optic atrophy; linked to a gene on chromosome 10q.

© Copyright 2016 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.
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