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