Savino P J, Glaser J S
Br J Ophthalmol. 1975 Dec;59(12):696-8. doi: 10.1136/bjo.59.12.696.
A child with opsoclonus associated with occult neuroblastoma is presented, in whom regression of the eye movement disorder through phases of flutter and dysmetria was observed. It is speculated that these ocular motor abnormalities represent a continuum of cerebellar dysfunction. A peculiar dysmetric head movemment not related to saccadic palsy is documented.
本文报告一名患有与隐匿性神经母细胞瘤相关的眼阵挛的儿童,观察到其眼球运动障碍通过震颤和辨距不良阶段逐渐消退。推测这些眼球运动异常代表小脑功能障碍的连续过程。记录了一种与眼球震颤性麻痹无关的特殊辨距不良性头部运动。