Wilson’s disease and the eye

Jyoti Rani Acharya, Paediatric Ophthalmology Fellow, K. Veena, Fredrick Mouttapa, Anjali Khadia, Paediatric Ophthalmology Consultant
{"title":"Wilson’s disease and the eye","authors":"Jyoti Rani Acharya, Paediatric Ophthalmology Fellow, K. Veena, Fredrick Mouttapa, Anjali Khadia, Paediatric Ophthalmology Consultant","doi":"10.17511/jooo.2019.i01.07","DOIUrl":null,"url":null,"abstract":"Wilson's disease is known for its rarity.It is inherited as an autosomal recessive trait and characterised by excessive accumulation of free copper in the body particularly the liver, brain, cornea and kidney. We report below a case of Wilson’s disease with well documented ocular findings. Incidental detection of K-F ring and Sunflower cataract by ophthalmologist in slit lamp examination in pre-symptomatic cases of Wilson’s disease may lead to early diagnosis and prompt management.","PeriodicalId":112259,"journal":{"name":"Tropical Journal of Ophthalmology and Otolaryngology","volume":"70 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tropical Journal of Ophthalmology and Otolaryngology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17511/jooo.2019.i01.07","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Wilson's disease is known for its rarity.It is inherited as an autosomal recessive trait and characterised by excessive accumulation of free copper in the body particularly the liver, brain, cornea and kidney. We report below a case of Wilson’s disease with well documented ocular findings. Incidental detection of K-F ring and Sunflower cataract by ophthalmologist in slit lamp examination in pre-symptomatic cases of Wilson’s disease may lead to early diagnosis and prompt management.
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
威尔逊氏病和眼睛
威尔逊氏病以罕见而闻名。它是一种常染色体隐性遗传性状,其特征是游离铜在体内过度积累,特别是在肝脏、大脑、角膜和肾脏。我们在此报告一个威尔森氏病的病例,有详细的眼部表现。在症状前的威尔逊氏病病例中,眼科医生在裂隙灯检查中偶然发现K-F环和向日葵白内障可能导致早期诊断和及时治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A retrospective study to analyse the ocular morbidity in the slum-dwelling population of central India. Sleep-disordered breathing a neglected risk factor in primary open-angle glaucoma Effect of donor and host factors on corneal graft transparency Clinical patterns of Uveitis in a Regional Eye Institute of North India Comparison of conjunctival free autograft and Rotational flap technique in primary pterygium surgery: Visual changes and safety profiles
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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