• 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

Genetics of hereditary vitreoretinal degenerations.

作者信息

Pachydaki Sophia I, Young Lucy H

机构信息

Ophthalmology Department, Retina Service, Massachusetts Eye and Ear Infirmary, Harvard Medical School, 243 Charles Street, Boston, MA 02114, USA.

出版信息

Semin Ophthalmol. 2007 Oct-Dec;22(4):219-27. doi: 10.1080/08820530701745132.

DOI:10.1080/08820530701745132
PMID:18097985
Abstract

The hereditary vitreoretinal disorders have variable vitreoretinal and other ocular and skeletal abnormalities. Some of these conditions represent a spectrum of clinical disease. This, along with the phenotypic variability, often leads to diagnostic difficulties. In this context, genetic testing is of valuable diagnostic value. Molecular genetic studies have helped distinguish conditions that were previously grouped together and proven others to represent spectrum of the same clinical entity. Accurate diagnosis is important in order to offer effective screening and genetic counseling and appropriate ophthalmological as well as systemic clinical surveillance.

摘要

相似文献

1
Genetics of hereditary vitreoretinal degenerations.
Semin Ophthalmol. 2007 Oct-Dec;22(4):219-27. doi: 10.1080/08820530701745132.
2
Snowflake vitreoretinal degeneration: follow-up of the original family.雪花状玻璃体视网膜变性:原家族的随访
Ophthalmology. 2003 Dec;110(12):2418-26. doi: 10.1016/S0161-6420(03)00828-5.
3
[Differential diagnosis of hereditary vitreoretinal degenerations ].[遗传性玻璃体视网膜变性的鉴别诊断]
Klin Monbl Augenheilkd. 1982 Jul;181(1):10-3. doi: 10.1055/s-2008-1055156.
4
Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome family.在一个大型斯-利综合征家族中鉴定出胶原蛋白2A1基因第2外显子中的一个终止密码子突变。
Am J Ophthalmol. 2002 Nov;134(5):720-7. doi: 10.1016/s0002-9394(02)01638-0.
5
[Classification of retinal degeneration in children].[儿童视网膜变性的分类]
Bull Soc Ophtalmol Fr. 1989 Aug-Sep;89(8-9):1027-33.
6
A phenotypic variant of Knobloch syndrome.诺布洛克综合征的一种表型变异型。
Ophthalmic Genet. 2008 Jun;29(2):85-6. doi: 10.1080/13816810701850041.
7
Hereditary vitreoretinal degenerations.遗传性玻璃体视网膜变性
Bull Soc Belge Ophtalmol. 1987;223 Pt 2:9-16.
8
Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 gene.斯-利二氏综合征的临床变异性:胶原COL2A1基因第2外显子的作用
Surv Ophthalmol. 2003 Mar-Apr;48(2):191-203. doi: 10.1016/s0039-6257(02)00460-5.
9
Molecular genetics of infantile-onset retinal dystrophies.婴儿期发病视网膜营养不良的分子遗传学
Eye (Lond). 2007 Oct;21(10):1344-51. doi: 10.1038/sj.eye.6702843.
10
Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14.伴有5号染色体q13-q14区域遗传连锁精细定位的瓦格纳玻璃体视网膜变性
Graefes Arch Clin Exp Ophthalmol. 1999 May;237(5):387-93. doi: 10.1007/s004170050249.

引用本文的文献

1
Clinical observations of vitreoretinal surgery for four different phenotypes of X-linked congenital retinoschisis.X连锁先天性视网膜劈裂四种不同表型的玻璃体视网膜手术临床观察
Int J Ophthalmol. 2018 Jun 18;11(6):986-990. doi: 10.18240/ijo.2018.06.15. eCollection 2018.