Yee R D, Duffin R M, Baloh R W, Isenberg S J
Arch Ophthalmol. 1982 Sep;100(9):1449-52. doi: 10.1001/archopht.1982.01030040427011.
Eye movements were studied in a sister and brother with familial, congenital paralysis of horizontal gaze. Horizontal and vertical eye movements were recorded with DC electro-oculography and analyzed with a laboratory computer. All horizontal, conjugate eye movements were absent (saccades, pursuit, optokinetic nystagmus, vestibulo-ocular response, and visual-vestibular responses). Voluntary vergence eye movements were preserved and were used to track visual targets. An involuntary, horizontal, pendular nystagmus was found to represent disconjugate, smooth, vergence eye movements. Vertical saccades and vestibulo-ocular responses were normal. However, vertical pursuit, optokinetic nystagmus, and suppression of the vestibulo-ocular response by fixation were impaired. A developmental anomaly affecting motor neurons and interneurons in the abducens nuclei is suggested to be the cause of the absence of conjugate, horizontal eye movements.
对一名患有家族性先天性水平凝视麻痹的姐妹和兄弟进行了眼动研究。采用直流眼电图记录水平和垂直眼动,并通过实验室计算机进行分析。所有水平共轭眼动均缺失(扫视、跟踪、视动性眼球震颤、前庭眼反射和视-前庭反射)。自主集合眼动得以保留,并用于跟踪视觉目标。发现一种不自主的水平摆动性眼球震颤代表非共轭、平滑的集合眼动。垂直扫视和前庭眼反射正常。然而,垂直跟踪、视动性眼球震颤以及注视对前庭眼反射的抑制受损。提示影响展神经核运动神经元和中间神经元的发育异常是共轭水平眼动缺失的原因。