先天性眼外肌纤维化:病例报告

Rahul Chaudhary, Prabha Sonwani, Suchita Singh
{"title":"先天性眼外肌纤维化:病例报告","authors":"Rahul Chaudhary, Prabha Sonwani, Suchita Singh","doi":"10.9734/or/2024/v19i3418","DOIUrl":null,"url":null,"abstract":"Unprogressive unilateral or bilateral limited ocular motility, with or without ptosis, is a hallmark of the uncommon congenital disease known as congenital fibrosis of extraocular muscle (CFEOM). Fibrosis of the extraocular muscle leads to optic nuclear dysplasia or hypoplasia and reduced ocular mobility, which in turn causes it. diverse phenotypes of illness might cause patients to report with diverse presentations.","PeriodicalId":287685,"journal":{"name":"Ophthalmology Research: An International Journal","volume":"19 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Congenital Fibrosis of Extraocular Muscles: A Case Report\",\"authors\":\"Rahul Chaudhary, Prabha Sonwani, Suchita Singh\",\"doi\":\"10.9734/or/2024/v19i3418\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Unprogressive unilateral or bilateral limited ocular motility, with or without ptosis, is a hallmark of the uncommon congenital disease known as congenital fibrosis of extraocular muscle (CFEOM). Fibrosis of the extraocular muscle leads to optic nuclear dysplasia or hypoplasia and reduced ocular mobility, which in turn causes it. diverse phenotypes of illness might cause patients to report with diverse presentations.\",\"PeriodicalId\":287685,\"journal\":{\"name\":\"Ophthalmology Research: An International Journal\",\"volume\":\"19 2\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ophthalmology Research: An International Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/or/2024/v19i3418\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ophthalmology Research: An International Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/or/2024/v19i3418","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

非进行性单侧或双侧眼球活动受限,伴有或不伴有上睑下垂,是眼外肌先天性纤维化(CFEOM)这种不常见的先天性疾病的特征。眼外肌纤维化会导致视神经核发育不良或发育不全以及眼球活动能力下降,进而引起眼球活动受限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Congenital Fibrosis of Extraocular Muscles: A Case Report
Unprogressive unilateral or bilateral limited ocular motility, with or without ptosis, is a hallmark of the uncommon congenital disease known as congenital fibrosis of extraocular muscle (CFEOM). Fibrosis of the extraocular muscle leads to optic nuclear dysplasia or hypoplasia and reduced ocular mobility, which in turn causes it. diverse phenotypes of illness might cause patients to report with diverse presentations.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Drug-induced Cornea Verticillata: A Report of 2 Cases Sustainable Development Goals and Eye Care in Nigeria Clinical Profile of Ocular Trauma at a Tertiary Care Hospital Amplitude of Accommodation in Young Caucasian Adults in Greece Antimicrobial and Immunostimulatory Effects of Senna occidentalis Ethanolic Extract against Aspergillus flavus-Induced Mycotic Keratitis: A Promising Therapeutic Approach
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1