Familial congenital oculomotor apraxia: Clinical and electro-oculographic features

被引:2
|
作者
Orssaud, Christophe [1 ,2 ]
Ingster-Moati, Isabelle [2 ]
Roche, Olivier [2 ]
Quoc, Emmanuel Bui [2 ]
Dufier, Jean Louis [2 ]
机构
[1] Hop Europeen Georges Pompidou, AP HP, Serv Ophtalmol, F-75015 Paris, France
[2] Hop Necker Enfants Malad, AP HP, Serv Ophtalmol, F-75015 Paris, France
关键词
Congenital oculomotor apraxia; Electrooculogram; Saccades; Pursuit; OCULAR MOTOR APRAXIA; JUVENILE NEPHRONOPHTHISIS; JOUBERT-SYNDROME; CHILDREN; FAILURE; NPHP1; TWINS;
D O I
10.1016/j.ejpn.2008.06.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The electro-oculographic (EOG) features of both horizontal and vertical eye movements in congenital oculomotor apraxia (COMA) were not previously reported. A girl referred to the ophthalmologic department for abnormal eye movements was diagnosed as COMA. The same abnormal ocular movements were observed in her younger sister and her father who was unaware of his difficulties to initiate voluntary saccades. When performed, EOG recordings of all horizontal and vertical saccadic eye movements were severely altered whatever the age of the patient. Pursuit was normal for these patients. It confirms that the control of saccadic eye movements is still altered in adults in both directions horizontal and vertical that were never reported. EOG is necessary to rule out inherited form of this saccade initiation failure. (C) 2008 European Paediatric Neurology Society.. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:370 / 372
页数:3
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