• 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

前房劈裂综合征。一种阶梯式分类法。

Anterior chamber cleavage syndrome. A stepladder classification.

作者信息

Waring G O, Rodrigues M M, Laibson P R

出版信息

Surv Ophthalmol. 1975 Jul-Aug;20(1):3-27. doi: 10.1016/0039-6257(75)90034-x.

DOI:10.1016/0039-6257(75)90034-x
PMID:808872
Abstract

This paper classifies the abnormalities of the anterior chamber cleavage syndrome (mesodermal dysgenesis of the iris and cornea). The anatomic findings are arranged in a tabular stepladder fashion which builds from simple to more complex combinations, most of which have been previously known by eponyms. There are three groups of anomalies: 1) peripheral, 2) central, and 3) combinations of the two. 1) The peripheral anomalies consist of a prominent Schwalbe's ring, iris strands to Schwalbe's ring, and hypoplasia of the anterior iris stroma. Developmental glaucoma is commonly present. 2) The essential feature of the central anomalies is a defect in the corneal endothelium and Descemet's membrane with an overlying corneal opacity. Additional components include central iridocorneal adhesions, keratolenticular approximation with cataract, and scleralizaiton of the cornea. Chorioretinal anomalies, developmental glaucoma, and systemic malformations may be present. 3) Central and peripheral combinations may exist in the same eye, in both eyes of the same patient, or within the same family.

摘要

本文对前房分裂综合征(虹膜和角膜的中胚层发育异常)的异常情况进行了分类。解剖学发现以表格阶梯形式排列,从简单到更复杂的组合,其中大多数以前都有其专属名称。有三组异常情况:1)周边型,2)中央型,3)两者的组合。1)周边异常包括突出的施瓦贝环、连接至施瓦贝环的虹膜条索以及虹膜前基质发育不全。通常伴有发育性青光眼。2)中央异常的基本特征是角膜内皮和后弹力层有缺陷,且上方有角膜混浊。其他成分包括中央虹膜角膜粘连、伴有白内障的角膜晶状体贴近以及角膜巩膜化。可能存在脉络膜视网膜异常、发育性青光眼和全身畸形。3)中央型和周边型组合可能存在于同一只眼睛、同一患者的双眼或同一家族内。

相似文献

1
Anterior chamber cleavage syndrome. A stepladder classification.前房劈裂综合征。一种阶梯式分类法。
Surv Ophthalmol. 1975 Jul-Aug;20(1):3-27. doi: 10.1016/0039-6257(75)90034-x.
2
Unilateral Rieger's anomaly.单侧里格尔异常
Am J Ophthalmol. 1980 Nov;90(5):725-7. doi: 10.1016/s0002-9394(14)75146-3.
3
Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome.Axenfeld-Rieger综合征:发病机制理论及与虹膜角膜内皮综合征的鉴别
Trans Am Ophthalmol Soc. 1983;81:736-84.
4
Anterior chamber cleavage syndrome. A typical case of Peters' anomaly with primary aphakia.前房劈裂综合征。彼得斯异常合并原发性无晶状体的典型病例。
Acta Ophthalmol (Copenh). 1972;50(6):877-86.
5
Axenfeld-Rieger syndrome. A spectrum of developmental disorders.阿克森费尔德-里格尔综合征。一系列发育障碍。
Surv Ophthalmol. 1985 May-Jun;29(6):387-409. doi: 10.1016/0039-6257(85)90205-x.
6
Congenital central corneal leukoma (Peters' anomaly).先天性中央角膜白斑(彼得斯异常)。
Am J Ophthalmol. 1976 Feb;81(2):173-93. doi: 10.1016/0002-9394(76)90729-7.
7
Mesodermal dysgenesis and hyaline membranes.中胚层发育不全与透明膜
Am J Ophthalmol. 1973 Oct;76(4):462-7. doi: 10.1016/0002-9394(73)90731-9.
8
Congenital corneal leukomas. 3. Histopathologic findings in 13 eyes with noncentral defect in Descemet's membrane.
Am J Ophthalmol. 1974 Mar;77(3):400-12.
9
Sclero-cornea and defective mesodermal migration.巩膜角膜与中胚层迁移缺陷。
Br J Ophthalmol. 1975 Nov;59(11):683-7. doi: 10.1136/bjo.59.11.683.
10
Unilateral Peters' anomaly complicated by a corneal tattoo.单侧彼得斯异常并发性角膜纹身。
Optom Vis Sci. 1998 Sep;75(9):635-9. doi: 10.1097/00006324-199809000-00017.

引用本文的文献

1
Pediatric corneal transplantation: techniques, challenges, and outcomes.小儿角膜移植:技术、挑战与结果
Ther Adv Ophthalmol. 2024 Mar 25;16:25158414241237906. doi: 10.1177/25158414241237906. eCollection 2024 Jan-Dec.
2
Classifications of anterior segment structure of congenital corneal opacity in infants and toddlers by ultrasound biomicroscopy and slit-lamp microscopic photographs: an observational study.先天性婴幼儿角膜混浊前节结构的超声生物显微镜和裂隙灯显微镜照片分类: 一项观察性研究。
BMC Ophthalmol. 2024 Jan 23;24(1):34. doi: 10.1186/s12886-024-03286-z.
3
Peters anomaly: An overview.
彼得斯异常:综述。
Taiwan J Ophthalmol. 2023 Oct 20;13(4):434-442. doi: 10.4103/tjo.TJO-D-23-00065. eCollection 2023 Oct-Dec.
4
Axenfeld-Rieger syndrome in monozygotic twin brothers: Case report.单卵双胞胎兄弟患阿克森费尔德-里格尔综合征:病例报告
North Clin Istanb. 2022 Aug 15;9(4):411-413. doi: 10.14744/nci.2021.89577. eCollection 2022.
5
Anterior synechiae after penetrating keratoplasty in infants and children with Peters' anomaly.婴幼儿先天性瞳孔残膜综合征行穿透性角膜移植术后前粘连
BMC Ophthalmol. 2022 Jun 9;22(1):259. doi: 10.1186/s12886-022-02473-0.
6
Glaucoma Syndromes: Insights into Glaucoma Genetics and Pathogenesis from Monogenic Syndromic Disorders.青光眼综合征:从单基因综合征性疾病看青光眼遗传学和发病机制。
Genes (Basel). 2021 Sep 11;12(9):1403. doi: 10.3390/genes12091403.
7
Surgical outcomes of Glaucoma associated with Axenfeld-Rieger syndrome.Axenfeld-Rieger 综合征相关青光眼的手术治疗效果。
BMC Ophthalmol. 2020 May 1;20(1):172. doi: 10.1186/s12886-020-01417-w.
8
Ultrasound Biomicroscopy Detects Peters' Anomaly and Rieger's Anomaly in Infants.超声生物显微镜检测婴儿彼得斯异常和里格尔异常。
J Ophthalmol. 2020 Mar 23;2020:8346981. doi: 10.1155/2020/8346981. eCollection 2020.
9
Primary congenital glaucoma: An updated review.原发性先天性青光眼:最新综述。
Saudi J Ophthalmol. 2019 Oct-Dec;33(4):382-388. doi: 10.1016/j.sjopt.2019.10.002. Epub 2019 Nov 7.
10
Pediatric cataract.小儿白内障
Indian J Ophthalmol. 2017 Dec;65(12):1340-1349. doi: 10.4103/ijo.IJO_1023_17.