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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.

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© Copyright 2018 Wolters Kluwer. All Rights Reserved. Review date: Sep 19, 2016.