Skip to Content

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.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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