| http://www.w3.org/ns/prov#value | - Following the original description of congenital oculomotor apraxia in children by Cogan,34,35 acquired oculomotor apraxia has been reported in various diseases, including types 2 and 3 GD, suggesting a brainstem or cerebellar origin for this finding.5,36 This case indicates that it may arise from an abnormality restricted to the dentate nucleus and its outflow.
|
