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Medical Term:

ataxia with oculomotor apraxia, I & II


Definition: two distinct autosomal recessive ataxias of childhood onset in which oculomotor apraxia is prominent. Both ataxias are due to gene mutations, with type II linked to a gene on chromosome 9q.

© Copyright 2017 Wolters Kluwer. All Rights Reserved. Review Date: Sep 19, 2016.