• 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

采用靶向基因测序对韩国原发性淋巴水肿患者进行临床分期和基因分析。

Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing.

机构信息

Department of Laboratory Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, South Korea.

Department of Plastic and Reconstructive Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, South Korea.

出版信息

Sci Rep. 2022 Aug 10;12(1):13591. doi: 10.1038/s41598-022-17958-7.

DOI:10.1038/s41598-022-17958-7
PMID:35948757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9365773/
Abstract

Lymphedema is a progressive disease caused by lymphatic flow blockage in the lymphatic pathway. Primary (hereditary) lymphedema is caused by genetic mutations without secondary causes. We performed clinical profiling on Korean primary lymphedema patients based on their phenotypes using lymphoscintigraphy and made genetic diagnoses using a next-generation sequencing panel consisting of 60 genes known to be related to primary lymphedema and vascular anomalies. Of 27 patients included in this study, 14.8% of the patients had lymphedema of the upper extremities, 77.8% had lymphedema of the lower extremities and 7.4% had 4-limbs lymphedema. Based on the International Society of Lymphology staging, 14, 10, and 3 patients had stage 3, 2, and 1 lymphedema, respectively. Only one family was genetically confirmed to harbor likely pathogenic variants in CELSR1. The proband was carrying two likely pathogenic variants in CELSR1, while her symptomatic mother was confirmed to carry only one of the variants. Furthermore, two other variants of uncertain significance in CELSR1 were detected in other patients, making CELSR1 the most commonly altered gene in our study. The clinical and genetic profile of hereditary lymphedema reported here is the first such data series reported for South Korea.

摘要

淋巴水肿是一种由淋巴通路中的淋巴液流动阻塞引起的进行性疾病。原发性(遗传性)淋巴水肿是由遗传突变引起的,没有继发性原因。我们基于淋巴闪烁显像对韩国原发性淋巴水肿患者进行了临床表型分析,并使用包含 60 个已知与原发性淋巴水肿和血管异常相关基因的下一代测序panel 进行了基因诊断。在这项研究中纳入的 27 名患者中,14.8%的患者上肢淋巴水肿,77.8%的患者下肢淋巴水肿,7.4%的患者四肢淋巴水肿。根据国际淋巴学会分期,分别有 14、10 和 3 名患者患有 3 期、2 期和 1 期淋巴水肿。只有一个家族在 CELSR1 中携带可能致病的变异。先证者携带 CELSR1 中的两个可能致病的变异,而其有症状的母亲仅携带一个变异。此外,在其他患者中还检测到 CELSR1 中的另外两个意义不明的变异,使 CELSR1 成为我们研究中最常改变的基因。这里报告的遗传性淋巴水肿的临床和遗传特征是韩国的首个此类数据系列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3290/9365773/28ffcf1ae9a4/41598_2022_17958_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3290/9365773/28ffcf1ae9a4/41598_2022_17958_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3290/9365773/28ffcf1ae9a4/41598_2022_17958_Fig1_HTML.jpg

相似文献

1
Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing.采用靶向基因测序对韩国原发性淋巴水肿患者进行临床分期和基因分析。
Sci Rep. 2022 Aug 10;12(1):13591. doi: 10.1038/s41598-022-17958-7.
2
Site Specific Evaluation of Lymphatic Vessel Sclerosis in Lower Limb Lymphedema Patients.下肢淋巴水肿患者淋巴管硬化的部位特异性评估
Lymphat Res Biol. 2018 Aug;16(4):360-367. doi: 10.1089/lrb.2017.0055. Epub 2018 Jan 17.
3
Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.越来越多的证据表明,CELSR1 功能丧失变异可导致遗传性淋巴水肿。
Am J Med Genet A. 2019 Sep;179(9):1718-1724. doi: 10.1002/ajmg.a.61269. Epub 2019 Jun 18.
4
Primary Lymphedema of the Upper Extremities: Clinical and Lymphoscintigraphic Features in 23 Patients.上肢原发性淋巴水肿:23例患者的临床和淋巴闪烁造影特征
Lymphat Res Biol. 2019 Feb;17(1):40-44. doi: 10.1089/lrb.2017.0085. Epub 2018 Oct 2.
5
Primary Lymphedema: Update on Genetic Basis and Management.原发性淋巴水肿:遗传基础与管理的最新进展
Adv Wound Care (New Rochelle). 2022 Jul;11(7):374-381. doi: 10.1089/wound.2020.1338. Epub 2021 Jan 27.
6
Rare PECAM1 variants in three families with lymphedema.三个淋巴水肿家族中的罕见PECAM1变异体。
Lymphology. 2020;53(3):141-151.
7
Three-Dimensional Imaging of Lymphatic System in Lymphedema Legs Using Interstitial Computed Tomography-lymphography.使用间质计算机断层扫描淋巴造影术对淋巴水肿腿部淋巴系统进行三维成像。
Acta Med Okayama. 2017 Apr;71(2):171-177. doi: 10.18926/AMO/54986.
8
Chy-3 mice are Vegfc haploinsufficient and exhibit defective dermal superficial to deep lymphatic transition and dermal lymphatic hypoplasia.Chy-3小鼠存在Vegfc单倍体不足,表现出从真皮浅层到深层淋巴管过渡缺陷以及真皮淋巴管发育不全。
Dev Dyn. 2007 Aug;236(8):2346-55. doi: 10.1002/dvdy.21208.
9
[Lymphedema secondary to breast cancer treatment: possibility of diagnostic and therapeutic prevention].[乳腺癌治疗继发淋巴水肿:诊断与治疗预防的可能性]
Ann Ital Chir. 2002 Sep-Oct;73(5):493-8.
10
[Frequency of lymphoscintigraphic anomalies in the contralateral limb and progression of unilateral primary lymphedema in children].[儿童对侧肢体淋巴闪烁造影异常的频率及单侧原发性淋巴水肿的进展]
Ann Dermatol Venereol. 2014 Nov;141(11):663-70. doi: 10.1016/j.annder.2014.06.022. Epub 2014 Aug 1.

引用本文的文献

1
Structural basis for regulation of CELSR1 by a compact module in its extracellular region.CELSR1胞外区域中一个紧密模块对其调控的结构基础。
Nat Commun. 2025 Apr 28;16(1):3972. doi: 10.1038/s41467-025-59319-8.
2
A Mutation in the Familial Case of Primary Lymphedema: A Report.家族性原发性淋巴水肿病例中的一个突变:报告。
Int J Mol Sci. 2024 May 17;25(10):5464. doi: 10.3390/ijms25105464.

本文引用的文献

1
Primary lymphoedema.原发性淋巴水肿。
Nat Rev Dis Primers. 2021 Oct 21;7(1):77. doi: 10.1038/s41572-021-00309-7.
2
Efficacy of Microsurgical Treatment of Primary Lymphedema: A Systematic Review.原发性淋巴水肿的显微外科治疗效果:系统评价。
Ann Plast Surg. 2022 Feb 1;88(2):195-199. doi: 10.1097/SAP.0000000000002862.
3
Lymphedema complicated by protein-losing enteropathy with a 22q13.3 deletion and the potential role of CELSR1: A case report.22q13.3 缺失导致蛋白丢失性肠病并发淋巴水肿:一例报告并探讨 CELSR1 的潜在作用。
Medicine (Baltimore). 2021 Jun 18;100(24):e26307. doi: 10.1097/MD.0000000000026307.
4
Primary Lymphedema: Update on Genetic Basis and Management.原发性淋巴水肿:遗传基础与管理的最新进展
Adv Wound Care (New Rochelle). 2022 Jul;11(7):374-381. doi: 10.1089/wound.2020.1338. Epub 2021 Jan 27.
5
Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second family.CELSR1 杂合性不足致女性淋巴水肿表现为性连锁不完全外显:第二家系。
Clin Genet. 2019 Nov;96(5):478-482. doi: 10.1111/cge.13622. Epub 2019 Aug 23.
6
Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.越来越多的证据表明,CELSR1 功能丧失变异可导致遗传性淋巴水肿。
Am J Med Genet A. 2019 Sep;179(9):1718-1724. doi: 10.1002/ajmg.a.61269. Epub 2019 Jun 18.
7
The Diagnosis and Treatment of Peripheral Lymphedema: 2016 Consensus Document of the International Society of Lymphology.外周性淋巴水肿的诊断与治疗:国际淋巴学会2016年共识文件
Lymphology. 2016 Dec;49(4):170-84.
8
Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach.采用新一代测序(NGS)方法对大量原发性淋巴水肿意大利患者队列进行基因筛查。
Lymphology. 2016 Jun;49(2):57-72.
9
Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema.VEGFC中的剪接位点突变导致功能丧失和非尼-米尔罗伊样原发性淋巴水肿。
Clin Genet. 2018 Jul;94(1):179-181. doi: 10.1111/cge.13204. Epub 2018 Mar 15.
10
A novel mutation in CELSR1 is associated with hereditary lymphedema.CELSR1基因的一种新突变与遗传性淋巴水肿相关。
Vasc Cell. 2016 Feb 5;8:1. doi: 10.1186/s13221-016-0035-5. eCollection 2016.