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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.

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

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