• 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

[先天性风疹的眼部表现]

[Ophthalmologic manifestations of congenital rubella].

作者信息

Merdassi A, Limaiem R, Turki F, Chaker N, Falfoul Y, Mghaieth F, Korchane N, Matri L El

机构信息

Institut d'ophtalmologie Hédi Rais de Tunis (Service B), 1006 Bab Saadoun, Tunis, Tunisie.

出版信息

Arch Pediatr. 2011 Aug;18(8):870-3. doi: 10.1016/j.arcped.2011.05.009. Epub 2011 Jun 12.

DOI:10.1016/j.arcped.2011.05.009
PMID:21665443
Abstract

Congenital rubella is a rare and serious disease including auditory neurological, cardiac, urinary, and ocular abnormalities. The eye complaints are often congenital cataract, congenital glaucoma, microphthalmia, and oculomotor disorders. We report the case of a 6-year-old girl presenting with a unilateral congenital cataract associated with congenital rubella. She was referred for complaints of high myopia in her right eye. She had a family history of cardiac and urogenital malformations, and presented deafness at birth. The ophthalmologic examination showed a microcornea and a unilateral dense congenital cataract in the right eye. B-scan ophthalmic ultrasound revealed a posterior microphthalmos. The anterior segment examination of the left eye was normal. Funduscopy revealed a salt-and-pepper appearance. Laboratory tests revealed a positive serology, confirming the congenital rubella. Given her complaints of loss of visual acuity in the right eye, the patient was operated on with a phacoaspiration implant in the capsular bag. The postoperative course was uneventful. The prevention of congenital rubella is based on routine vaccination of children. The association of cataract, congenital heart defects, and deafness must be systematically investigated as it may be more serious in association with systemic manifestations.

摘要

先天性风疹是一种罕见且严重的疾病,包括听觉神经、心脏、泌尿和眼部异常。眼部症状通常为先天性白内障、先天性青光眼、小眼症和动眼障碍。我们报告一例6岁女孩,患有与先天性风疹相关的单侧先天性白内障。她因右眼高度近视前来就诊。她有心脏和泌尿生殖系统畸形的家族史,出生时即有耳聋。眼科检查显示右眼角膜微小,存在单侧致密先天性白内障。B超眼部超声检查显示后部小眼症。左眼眼前节检查正常。眼底检查显示椒盐样外观。实验室检查血清学呈阳性,确诊为先天性风疹。鉴于她右眼视力下降的症状,患者接受了囊袋内超声乳化植入手术。术后过程顺利。先天性风疹的预防基于儿童常规疫苗接种。白内障、先天性心脏缺陷和耳聋的关联必须进行系统调查,因为与全身表现相关时可能更为严重。

相似文献

1
[Ophthalmologic manifestations of congenital rubella].[先天性风疹的眼部表现]
Arch Pediatr. 2011 Aug;18(8):870-3. doi: 10.1016/j.arcped.2011.05.009. Epub 2011 Jun 12.
2
Ocular manifestations of congenital rubella syndrome in a developing country.发展中国家先天性风疹综合征的眼部表现
Indian J Ophthalmol. 2002 Dec;50(4):307-11.
3
[Manifestation of congenital rubella syndrome: clinical and epidemiologic aspects].[先天性风疹综合征的表现:临床与流行病学方面]
Bull Soc Belge Ophtalmol. 2007(303):13-20.
4
Congenital rubella syndrome: ophthalmic manifestations and associated systemic disorders.先天性风疹综合征:眼部表现及相关全身性疾病
Br J Ophthalmol. 1993 Jun;77(6):358-63. doi: 10.1136/bjo.77.6.358.
5
An epidemiological and clinical study of ocular manifestations of congenital rubella syndrome in Omani children.阿曼儿童先天性风疹综合征眼部表现的流行病学与临床研究。
Arch Ophthalmol. 2004 Apr;122(4):541-5. doi: 10.1001/archopht.122.4.541.
6
Central serous chorioretinopathy after trabeculectomy in a patient with microphthalmos and congenital rubella syndrome.
Retin Cases Brief Rep. 2014 Spring;8(2):153-6. doi: 10.1097/ICB.0000000000000029.
7
Visual outcome of cataract surgery in children with congenital rubella syndrome.先天性风疹综合征患儿白内障手术的视觉预后。
J AAPOS. 2003 Apr;7(2):91-5. doi: 10.1016/mpa.2003.S1091853102420022.
8
Optical complications in congenital rubella syndrome.先天性风疹综合征的眼部并发症。
Optometry. 2002 Jul;73(7):418-24.
9
Secondary congenital aphakia.继发性先天性无晶状体
Rom J Ophthalmol. 2016 Jan-Mar;60(1):37-9.
10
Congenital ocular malformations (lens subluxation, pupillary displacement, cataract, myopia) and classic galactosaemia associated with Q188R and /or G1391A mutations.先天性眼部畸形(晶状体半脱位、瞳孔移位、白内障、近视)与 Q188R 和/或 G1391A 突变相关的经典半乳糖血症。
Acta Ophthalmol. 2011 Aug;89(5):489-94. doi: 10.1111/j.1755-3768.2009.01691.x. Epub 2010 Mar 10.

引用本文的文献

1
Volume of Structures in the Fetal Brain Measured with a New Semiautomated Method.使用新半自动方法测量胎儿脑内结构容积。
AJNR Am J Neuroradiol. 2017 Nov;38(11):2193-2198. doi: 10.3174/ajnr.A5349. Epub 2017 Aug 24.
2
Detection of TORCH pathogens in children with congenital cataracts.先天性白内障患儿中TORCH病原体的检测
Exp Ther Med. 2016 Aug;12(2):1159-1164. doi: 10.3892/etm.2016.3348. Epub 2016 May 17.