• 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

Axenfeld-Rieger 综合征相关的眼压升高。

Ocular hypertension in Axenfeld-Rieger Syndrome.

机构信息

Institut Català de Retina, Barcelona, Spain.

Postgraduate and Doctorate School, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain.

出版信息

Rom J Ophthalmol. 2020 Oct-Dec;64(4):455-458. doi: 10.22336/rjo.2020.70.

DOI:10.22336/rjo.2020.70
PMID:33367186
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7739019/
Abstract

to describe a clinical case of ocular hypertension (OHT) in Axenfeld-Rieger Syndrome (ARS). Observational case report of a 43-year-old woman with background of OHT. The data was collected originally with a standardized electronic medical record. A complete ophthalmologic examination was performed. In the biomicroscopy, a posterior embryotoxon, iris atrophy with absence of crypts and irregularity of pigmentation, and discoria in OU were observed. Gonioscopy revealed an open angle with a prominent and anterior displaced Schwalbe line. Ocular fundus (OF) demonstrated small and oblique papillae, with normal neurorretinal ring. Functional tests were normal. The patient did not present systemic pathologies, so the diagnosis of Rieger anomaly was made. The IOP control was achieved with aqueous humor suppressants. Glaucoma is the main cause of visual morbidity in patients with ARS, therefore a complete periodic ophthalmological exam is a priority. :ARS = Axenfeld-Rieger Syndrome, RP = retinitis pigmentosa, IOP = Intraocular Pressure, BCVA = Best Corrected Visual Acuity, OR = right eye, OS = left eye, OU = both eyes, OF = ocular fundus, OCT = optical coherence tomography, VF = visual field, TBC = trabeculectomy.

摘要

描述 Axenfeld-Rieger 综合征(ARS)伴发的眼压升高(OHT)的临床病例。 对一名 43 岁女性 OHT 背景下的观察性病例报告。数据最初是通过标准化电子病历收集的。进行了全面的眼科检查。在眼前节检查中,观察到后胚胎性突、虹膜萎缩伴隐窝缺失和色素沉着不规则,双眼均存在虹膜异色。房角镜检查显示宽角伴 Schwalbe 线明显向前移位。眼底(OF)显示小而倾斜的视乳头,神经视网膜环正常。功能检查正常。患者未出现全身系统性疾病,因此诊断为 Rieger 异常。通过房水抑制剂控制眼压。 青光眼是 ARS 患者视力损害的主要原因,因此全面定期眼科检查是首要任务。 :ARS = Axenfeld-Rieger 综合征,RP = 色素性视网膜炎,IOP = 眼内压,BCVA = 最佳矫正视力,OR = 右眼,OS = 左眼,OU = 双眼,OF = 眼底,OCT = 光学相干断层扫描,VF = 视野,TBC = 小梁切除术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/7739019/4140aea90ad2/RomJOphthalmol-64-455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/7739019/3723dc4a88ce/RomJOphthalmol-64-455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/7739019/4140aea90ad2/RomJOphthalmol-64-455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/7739019/3723dc4a88ce/RomJOphthalmol-64-455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1bb/7739019/4140aea90ad2/RomJOphthalmol-64-455-g002.jpg

相似文献

1
Ocular hypertension in Axenfeld-Rieger Syndrome.Axenfeld-Rieger 综合征相关的眼压升高。
Rom J Ophthalmol. 2020 Oct-Dec;64(4):455-458. doi: 10.22336/rjo.2020.70.
2
Progressive High Hypermetropic Shift as a Refractive Surprise Following Glaucoma Filtration Surgery in a Phakic Child With Early-Onset Childhood Glaucoma Associated With Axenfeld-Rieger Anomaly.先天性青光眼伴 Axenfeld-Rieger 异常患儿行青光眼滤过手术后出现进行性高度远视漂移:一种屈光意外
J Glaucoma. 2019 Aug;28(8):e136-e139. doi: 10.1097/IJG.0000000000001283.
3
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.
4
Double trouble: Microspherophakia with Axenfeld-Rieger anomaly.双重麻烦:伴有Axenfeld-Rieger异常的小球形晶状体。
Indian J Ophthalmol. 2019 Mar;67(3):394-395. doi: 10.4103/ijo.IJO_978_18.
5
Axenfeld-Rieger syndrome combined with a foveal anomaly in a three-generation family: a case report.三代家系中 Axenfeld-Rieger 综合征合并中心凹异常 1 例报告
BMC Ophthalmol. 2021 Mar 29;21(1):154. doi: 10.1186/s12886-021-01899-2.
6
Unusual presentation in Axenfeld-Rieger syndrome.Axenfeld-Rieger 综合征的不典型表现。
Indian J Ophthalmol. 2011 Jul-Aug;59(4):312-4. doi: 10.4103/0301-4738.82003.
7
[Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].[阿克森费尔德-里格尔综合征家族中的临床表现变异性]
Klin Oczna. 2007;109(7-9):321-6.
8
High Iris Insertion in Axenfeld-Rieger Syndrome.Axenfeld-Rieger综合征中的高虹膜附着
Ophthalmology. 2020 Jun;127(6):768. doi: 10.1016/j.ophtha.2020.02.012.
9
Axenfeld-Rieger syndrome: A case report.阿克森费尔德-里格尔综合征:一例报告。
J Fr Ophtalmol. 2019 Apr;42(4):e157-e158. doi: 10.1016/j.jfo.2018.08.014. Epub 2019 Mar 21.
10
[Embryotoxon in Axenfeld-Rieger syndrome in an infant].[婴儿Axenfeld-Rieger综合征中的胚胎环]
J Fr Ophtalmol. 2018 Jan;41(1):100-101. doi: 10.1016/j.jfo.2017.08.004. Epub 2017 Dec 11.

本文引用的文献

1
Progressive High Hypermetropic Shift as a Refractive Surprise Following Glaucoma Filtration Surgery in a Phakic Child With Early-Onset Childhood Glaucoma Associated With Axenfeld-Rieger Anomaly.先天性青光眼伴 Axenfeld-Rieger 异常患儿行青光眼滤过手术后出现进行性高度远视漂移:一种屈光意外
J Glaucoma. 2019 Aug;28(8):e136-e139. doi: 10.1097/IJG.0000000000001283.
2
Axenfeld-Rieger syndrome.Axenfeld-Rieger 综合征。
Clin Genet. 2018 Jun;93(6):1123-1130. doi: 10.1111/cge.13148. Epub 2018 Jan 25.
3
Unclassified Axenfeld-Rieger Syndrome: A CASE SERIES and Review of Literature.
未分类的Axenfeld-Rieger综合征:病例系列及文献综述
Semin Ophthalmol. 2018;33(3):300-307. doi: 10.1080/08820538.2016.1208767. Epub 2016 Dec 8.
4
Early-onset glaucoma in Axenfeld-Rieger anomaly: long-term surgical results and visual outcome.Axenfeld-Rieger异常综合征中的早发性青光眼:长期手术结果及视力转归
Eye (Lond). 2016 Jul;30(7):936-42. doi: 10.1038/eye.2016.66. Epub 2016 Apr 8.
5
Axenfeld-Rieger syndrome: a case report.阿克森费尔德-里格尔综合征:一例病例报告。
J Orthod. 2015;42(4):324-30. doi: 10.1179/1465313315Y.0000000017. Epub 2015 Aug 18.
6
Axenfeld-Rieger syndrome and spectrum of PITX2 and FOXC1 mutations.Axenfeld-Rieger 综合征及 PITX2 和 FOXC1 基因突变谱。
Eur J Hum Genet. 2009 Dec;17(12):1527-39. doi: 10.1038/ejhg.2009.93. Epub 2009 Jun 10.
7
Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.Axenfeld-Rieger畸形及伴有FOXC1和PITX2突变的青光眼患者的基因型-表型相关性
Invest Ophthalmol Vis Sci. 2007 Jan;48(1):228-37. doi: 10.1167/iovs.06-0472.
8
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis.FOXC1与PITX2之间的功能相互作用是Axenfeld-Rieger综合征和眼前节发育异常中对FOXC1基因剂量敏感性的基础。
Hum Mol Genet. 2006 Mar 15;15(6):905-19. doi: 10.1093/hmg/ddl008. Epub 2006 Jan 31.