• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Congenital ocular motor apraxia in twins. Findings with magnetic resonance imaging.

作者信息

Borchert M S, Sadun A A, Sommers J D, Wright K W

出版信息

J Clin Neuroophthalmol. 1987 Jun;7(2):104-7.

PMID:2956282
Abstract

A pair of identical twins, whose features met Cogan's classic description of congenital ocular motor apraxia, were examined. Each had an absence of willed horizontal saccades and demonstrated classic head thrusting. Magnetic resonance imaging revealed hypoplasia of the corpus callosum. Fourth ventricle enlargement and generalized cerebral hypoplasia were also present but were more pronounced in the sibling with the more delayed motor development. The significance of these findings is discussed in light of our understanding of the control mechanism of volitional eye movements.

摘要

相似文献

1
Congenital ocular motor apraxia in twins. Findings with magnetic resonance imaging.
J Clin Neuroophthalmol. 1987 Jun;7(2):104-7.
2
Spasmus nutans and congenital ocular motor apraxia with cerebellar vermian hypoplasia.点头痉挛与伴有小脑蚓部发育不全的先天性眼球运动失用症。
Arch Neurol. 2003 Nov;60(11):1621-4. doi: 10.1001/archneur.60.11.1621.
3
[Twins with congenital oculomotor apraxia (Cogan's syndrome)].
Klin Monbl Augenheilkd. 1979 Sep;175(3):360-6.
4
Congenital ocular motor apraxia in two siblings.两名兄弟姐妹患先天性眼球运动失用症。
Pediatr Neurol. 1995 Oct;13(3):261-2. doi: 10.1016/0887-8994(95)00182-f.
5
Congenital ocular motor apraxia: sporadic and familial. Support for natural resolution.
J Neuroophthalmol. 1994 Jun;14(2):102-4.
6
[Congenital oculomotor apraxia. Presentation--developmental problems--differential diagnosis].
Klin Monbl Augenheilkd. 1992 May;200(5):623-5. doi: 10.1055/s-2008-1045846.
7
Acquired ocular motor apraxia due to bilateral frontoparietal infarcts.
Ann Neurol. 1988 Feb;23(2):199-202. doi: 10.1002/ana.410230216.
8
Congenital ocular motor apraxia.先天性眼球运动失用症。
Trans Ophthalmol Soc U K (1962). 1986;105 ( Pt 5):589-98.
9
Congenital ocular motor apraxia associated with idiopathic generalized epilepsy in monozygotic twins.单卵双胞胎中与特发性全身性癫痫相关的先天性眼球运动失用症。
Dev Med Child Neurol. 2004 Jun;46(6):428-30. doi: 10.1017/s0012162204000696.
10
Congenital ocular motor apraxia with autosomal dominant inheritance.
Am J Ophthalmol. 2000 Jun;129(6):820-2. doi: 10.1016/s0002-9394(00)00373-1.

引用本文的文献

1
Intermittent horizontal saccade failure ('ocular motor apraxia') in children.儿童间歇性水平扫视功能障碍(“眼球运动性失用症”)
Br J Ophthalmol. 1996 Feb;80(2):151-8. doi: 10.1136/bjo.80.2.151.