Neurodevelopmental implications of ocular motor apraxia
Article first published online: 13 FEB 2007
Developmental Medicine & Child Neurology
Volume 47, Issue 12, pages 815–819, December 2005
How to Cite
Marr, J. E., Green, S. H. and Willshaw, H. (2005), Neurodevelopmental implications of ocular motor apraxia. Developmental Medicine & Child Neurology, 47: 815–819. doi: 10.1111/j.1469-8749.2005.tb01086.x
- Issue published online: 13 FEB 2007
- Article first published online: 13 FEB 2007
- Accepted for publication 14th December 2004.
Ocular motor apraxia (OMA), a disorder of saccadic initiation, may be congenital or acquired. While the acquired form is frequently associated with significant neuropathology, the congenital form is often regarded as relatively benign. Many children with congenital OMA who were observed clinically have shown neurodevelopmental disturbance over time. A retrospective review was taken of 34 consecutive patients (22 males and 12 females), seen over a 20–year period, to evaluate the frequency and type of associated neurodevelopmental problems. Age at presentation ranged from 8 weeks to 14 years, with a mean age of 10 years. Of 29 children with congenital OMA, 15 had imaging evidence of structural central nervous system abnormalities (with cerebellar hypoplasia the most frequent abnormality detected). Eleven of the 14 patients with no structural abnormality showed abnormal neurodevelopment. This study suggests that congenital OMA is not a benign diagnosis, even in the absence of overt neurological disturbance at the time of presentation.