国际眼科纵览 ›› 2020, Vol. 44 ›› Issue (5): 296-305.doi: 10.3760/ cma.j.issn.1673-5803.2020.05.002

• 综述 • 上一篇    下一篇

先天性眼球震颤的研究进展

刘彦孜 史学锋   

  1. 天津医科大学眼科临床学院  天津市眼科医院  天津市眼科研究所  天津市眼科学与视觉科学重点实验室 300020
  • 收稿日期:2020-05-20 出版日期:2020-10-22 发布日期:2020-11-01
  • 通讯作者: 史学锋,Email:shixf_tmu@163.com
  • 基金资助:
    国家自然科学基金(81770956,81371049);天津市杰出青年科学基金(17JCJQJC46000);天津市卫生计生行业高层次人才选拔培养工程“津门医学英才”项目

Research progress on congenital nystagmus

Liu Yanzi, Shi Xuefeng   

  1. Clinical College of Ophthalmology of Tianjin Medical University, Tianjin Eye Hospital and Institute, Tianjin Key Laboratory of Ophthalmology and Visual Science, Tianjin 300020, China
  • Received:2020-05-20 Online:2020-10-22 Published:2020-11-01
  • Contact: Shi Xuefeng, Email: shixf_tmu@163.com
  • Supported by:
    National Natural Science Foundation of China (81770956, 81371049); Tianjin Science Foundation for Distinguished Young Scholars (17JCJQJC46000); Jinmen Medical Talent Project of Tianjin Health Commission

摘要: 先天性眼球震颤(congenital nystagmus,CN)是一种双眼不自主的、有节律的眼球摆动,常于刚出生时或出生后3个月内发现。CN的病因复杂多样,迄今其发病机制尚未完全清楚,属于斜视与小儿眼科疑难性疾病,治疗较为困难。近年来,国际同行尝试对原有术式进行改进,以期让患者获得更好的视觉质量。临床随机对照研究发现一些药物可减轻眼球震颤强度,延长中心凹注视时间,并使患者视力提高。CN的遗传方式多样,目前多数CN致病基因导致发病的机制尚不清楚。通过对模式动物的研究现已揭示了X连锁CN的致病基因——FRMD7基因引起CN的机制与方向选择性视网膜神经节细胞对水平方向运动的检测功能丧失有关。本文对近年来CN的研究进展进行综述,以期为CN的临床和基础研究提供参考。(国际眼科纵览,2020, 44: 296-305)

关键词: 先天性眼球震颤, 手术治疗, 药物治疗, 遗传学, 发病机制

Abstract: Congenital nystagmus (CN) is an involuntary, rhythmic ocular oscillations that is often detected at birth or within 3 months of birth. The etiology of CN is complex and diverse. Till now, the pathogenesis of CN has not been entirely clear. CN is a difficult disease in the clinic of pediatric ophthalmology and strabismus, its treatment is difficult. In recent years, researchers have tried to improve the original surgical procedures in order to give patients better visual quality. Randomized, controlled, double-blind clinical studies have found that some drugs can reduce nystagmus intensity, prolong foveal fixation, and improve vision in patients. The genetic modes of CN are varied, and the pathogenesis of most of the CN is still unclear. Studies on model animals have revealed that the mechanism by which the FRMD7 gene, one of the pathogenic genes of X-linked CN,  is related to the loss of horizontal motion detection of direction selective retinal ganglion cells. This article reviews the recent progress research of CN in order to provide references for future clinical and basic studies. (Int Rev Ophthalmol, 2020, 44:  296-305)

Key words: congenital nystagmus, surgical treatment, drug therapy, genetics, pathogenesis