两名兄弟姐妹患先天性眼球运动失用症。

Congenital ocular motor apraxia in two siblings.

作者信息

Gürer Y K, Kükner S, Kunak B, Yilmaz S

机构信息

Dr. Sami Ulus Children's Hospital, Ankara, Turkey.

出版信息

Pediatr Neurol. 1995 Oct;13(3):261-2. doi: 10.1016/0887-8994(95)00182-f.

DOI:10.1016/0887-8994(95)00182-f

PMID:8554667

Abstract

Two siblings whose features met Cogan's classic description of congenital ocular motor apraxia were examined. There was first-degree consanguinity in the family. Each had an absence of voluntary and optically-induced horizontal eye movements and demonstrated classic head thrusting.

摘要

对两名特征符合科根先天性眼球运动失用经典描述的兄弟姐妹进行了检查。该家族存在一级近亲结婚情况。两人均缺乏自主和视动性水平眼球运动，并表现出典型的头部前推动作。