• 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

中国先天性晶状体异位患者中双等位基因 ADAMTSL4 变异:对基因型-表型关系的影响。

Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships.

机构信息

Eye Institute and Department of Ophthalmology, Eye & ENT Hospital, Fudan University, Shanghai, China.

NHC Key Laboratory of Myopia (Fudan University); Key Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China.

出版信息

Hum Mutat. 2022 Dec;43(12):2141-2152. doi: 10.1002/humu.24483. Epub 2022 Oct 17.

DOI:10.1002/humu.24483
PMID:36208099
Abstract

ADAMTSL4 variants are one of the common causes of congenital ectopia lentis (EL), reported ocular comorbidities of which include iris anomalies, cataract, and glaucoma. However, a genotype-phenotype correlation has not been established. Potentially pathogenic ADAMTSL4 variants were screened from a Chinese cohort of congenital EL using panel-based next-generation sequencing followed by multiple bioinformatics analyses. The genotype-phenotype correlation was assessed via a systematic review of ADAMTSL4 variants within our data and those from the literature. A total of 12 variants of ADAMTSL4, including seven frameshift variants, one nonsense variant, two splicing variants, and two missense variants, were found in nine probands. Combing genetic and clinical information from 72 probands in the literature revealed 37 ADAMTSL4 variants known to cause EL, and the ethnic difference was prominent. The lens was inclined to dislocate inferior temporally (22, 27.16%), while the pupil was always located oppositely (9, 81.82%). Several anterior segments anomalies were identified, including ectopia pupillae (15, 18.52%), persistent pupillary membrane (9, 11.10%), poor pupil dilation (4, 30.8%), cataract (13, 24.10%), and glaucoma (8, 13.33%). Genotype-phenotype analysis revealed that truncation variants had higher risks of combined iris anomalies, including either ectopia pupillae or a persistent pupillary membrane (p =  0.007). The data from this study not only extend our knowledge of the ADAMTSL4 variant spectrum but also suggest that deleterious variants of ADAMTSL4 might be associated with severe ocular phenotypes.

摘要

ADAMTSL4 变异是先天性晶状体异位 (EL) 的常见原因之一,已报道其眼部合并症包括虹膜异常、白内障和青光眼。然而,尚未建立基因型-表型相关性。使用基于面板的下一代测序对先天性 EL 的中国队列进行筛选,然后进行多次生物信息学分析,以筛选潜在的致病性 ADAMTSL4 变异。通过对我们数据中 ADAMTSL4 变异和文献中 ADAMTSL4 变异的系统综述,评估基因型-表型相关性。在九个先证者中发现了 12 种 ADAMTSL4 变异,包括 7 种移码变异、1 种无义变异、2 种剪接变异和 2 种错义变异。结合文献中 72 个先证者的遗传和临床信息,发现了 37 种已知引起 EL 的 ADAMTSL4 变异,且种族差异明显。晶状体倾向于颞下脱位(22,27.16%),而瞳孔总是位于对侧(9,81.82%)。确定了几种前节异常,包括瞳孔异位(15,18.52%)、永存瞳孔膜(9,11.10%)、瞳孔扩张不良(4,30.8%)、白内障(13,24.10%)和青光眼(8,13.33%)。基因型-表型分析表明,截断变异与联合虹膜异常的风险更高,包括瞳孔异位或永存瞳孔膜(p=0.007)。本研究的数据不仅扩展了我们对 ADAMTSL4 变异谱的认识,还表明 ADAMTSL4 的有害变异可能与严重的眼部表型相关。

相似文献

1
Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships.中国先天性晶状体异位患者中双等位基因 ADAMTSL4 变异:对基因型-表型关系的影响。
Hum Mutat. 2022 Dec;43(12):2141-2152. doi: 10.1002/humu.24483. Epub 2022 Oct 17.
2
The phenotypic spectrum of associated ectopia lentis: Additional cases, complications, and review of literature.相关晶状体异位表型谱:附加病例、并发症及文献复习。
Mol Vis. 2022 Sep 4;28:257-268. eCollection 2022.
3
Novel gene mutations in Chinese patients with isolated ectopia lentis.中国单纯晶状体异位患者的新型基因突变
Br J Ophthalmol. 2023 Jun;107(6):774-779. doi: 10.1136/bjophthalmol-2021-320475. Epub 2022 Jan 18.
4
Correlation between novel compound heterozygous ADAMTSL4 variants and primary phenotypes of ectopia lentis et pupillae.新型 ADAMTSL4 复合杂合变体与晶状体异位和瞳孔异常的主要表型之间的相关性。
Exp Eye Res. 2022 Nov;224:109243. doi: 10.1016/j.exer.2022.109243. Epub 2022 Sep 9.
5
A novel ADAMTSL4 mutation in autosomal recessive ectopia lentis et pupillae.常染色体隐性晶状体异位和瞳孔异位的新型 ADAMTSL4 突变。
Invest Ophthalmol Vis Sci. 2010 Dec;51(12):6369-73. doi: 10.1167/iovs.10-5597. Epub 2010 Aug 11.
6
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians.晶状体异位中ADAMTSL4评估揭示了波利尼西亚人存在反复出现的始祖突变。
Ophthalmic Genet. 2017 Dec;38(6):537-543. doi: 10.1080/13816810.2017.1309552. Epub 2017 Apr 10.
7
A genotype-phenotype comparison of ADAMTSL4 and FBN1 in isolated ectopia lentis.ADAMTSL4 和 FBN1 在单纯性晶状体异位中的基因型-表型比较。
Invest Ophthalmol Vis Sci. 2012 Jul 24;53(8):4889-96. doi: 10.1167/iovs.12-9874.
8
ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent.与ADAMTSL4相关的晶状体异位:一例具有无症状亲代的假显性病例。
Am J Med Genet A. 2022 Jun;188(6):1853-1857. doi: 10.1002/ajmg.a.62698. Epub 2022 Feb 26.
9
Ectopia Lentis et Pupillae Caused by ADAMTSL4 Pathogenic Variants and an Algorithm for Work-up.由ADAMTSL4致病变异引起的晶状体和瞳孔异位及检查算法
J Pediatr Ophthalmol Strabismus. 2019 Jul 5;56:e45-e48. doi: 10.3928/01913913-20190509-01.
10
A novel ADAMTSL4 compound heterozygous mutation in isolated ectopia lentis: a case report and review of the literature.孤立性晶状体异位的新型 ADAMTSL4 复合杂合突变:病例报告及文献复习。
J Med Case Rep. 2023 Dec 26;17(1):532. doi: 10.1186/s13256-023-04272-7.

引用本文的文献

1
Genetic landscape and ocular biometric correlations in microspherophakia: insights from a comprehensive patient cohort.小眼球症的遗传图谱与眼生物测量相关性:来自一个综合患者队列的见解
Hum Genomics. 2025 Mar 1;19(1):22. doi: 10.1186/s40246-025-00729-6.