Two Cases of Congenital Ocular Motor Apraxia Associated With Cerebellar Vermian Dysplasia.
- Author:
Jin Young SEO
1
;
Yeon Hee LEE
;
Byoung Soo SHIN
;
Man Wook SEO
;
Young Hyun KIM
;
Sun Young OH
Author Information
1. Department of Neurology, College of Medicine, Chonbuk National University, Korea. ohsun@chonbuk.ac.kr
- Publication Type:Case Report
- Keywords:
Congenital ocular motor apraxia;
Joubert's syndrome;
Oculography
- MeSH:
Apraxias;
Child;
Cogan Syndrome;
Eye Movements;
Head;
Humans;
Magnetic Resonance Imaging
- From:Journal of the Korean Balance Society
2008;7(1):63-67
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Congenital ocular motor apraxia is a rare syndrome characterized by rotational head thrusts that attempt to compensate for the lack of voluntary eye movements. We describe the clinical, oculographic and magnetic resonance imaging features of two children with congenital ocular motor apraxia.
