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一名患有肺泡毛细血管发育不良伴肺静脉错位的新生儿中FOXF1基因的一种新型新生致病性变异

A Novel De Novo Pathogenic Variant in FOXF1 in a Newborn with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins.

作者信息

Ma Youngeun, Jang Mi Ae, Yoo Hye Soo, Ahn So Yoon, Sung Se In, Chang Yun Sil, Ki Chang Seok, Park Won Soon

机构信息

Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Department of Laboratory Medicine and Genetics, Soonchunhyang University Bucheon Hospital, Soonchunhyang University College of Medicine, Bucheon, Korea.

出版信息

Yonsei Med J. 2017 May;58(3):672-675. doi: 10.3349/ymj.2017.58.3.672.

DOI:10.3349/ymj.2017.58.3.672
PMID:28332379
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5368159/
Abstract

Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is an autosomal dominant, fatal developmental disorder of the lungs, with a mortality rate of about 100%. ACD/MPV is caused by mutations in FOXF1. Herein, we describe a newborn boy with ACD/MPV carrying a novel pathogenic variant of FOXF1. The patient developed respiratory distress and severe pulmonary hypertension on the first day of life. Despite aggressive cardiorespiratory management, including veno-venous extracorporeal membrane oxygenation, his condition deteriorated rapidly, and he died within the first month of his life. Lung histology showed the characteristic features of ACD/MPV at autopsy. Sequence analysis of FOXF1 from genomic DNA obtained from autopsied lung tissue revealed that the patient was heterozygous for a novel missense variant (c.305T>C; p.Leu102Pro). Further analysis of both parents confirmed the de novo occurrence of the variant. To the best of our knowledge, this is the first report of genetically confirmed ACD/MPV in Korea.

摘要

肺泡毛细血管发育不良伴肺静脉异位引流(ACD/MPV)是一种常染色体显性遗传的致命性肺部发育障碍疾病,死亡率约为100%。ACD/MPV由FOXF1基因突变引起。在此,我们描述了一名患有ACD/MPV的男婴,其携带FOXF1基因的一种新型致病变体。该患者在出生第一天就出现了呼吸窘迫和严重的肺动脉高压。尽管采取了积极的心肺管理措施,包括静脉-静脉体外膜肺氧合,但他的病情迅速恶化,在出生后第一个月内死亡。尸检时肺组织学显示出ACD/MPV的特征性表现。对从尸检肺组织获得的基因组DNA进行FOXF1序列分析发现,该患者为一种新型错义变体(c.305T>C;p.Leu102Pro)的杂合子。对其父母的进一步分析证实了该变体的新发情况。据我们所知,这是韩国首例经基因确诊的ACD/MPV报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/c15e0845ae36/ymj-58-672-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/2710767e53bf/ymj-58-672-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/2b22ba02c76d/ymj-58-672-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/c15e0845ae36/ymj-58-672-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/2710767e53bf/ymj-58-672-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/2b22ba02c76d/ymj-58-672-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3629/5368159/c15e0845ae36/ymj-58-672-g003.jpg

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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.序列变异解读的标准与指南:美国医学遗传学与基因组学学会和分子病理学协会的联合共识推荐
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高度敏感的阻断剂置换扩增和液滴数字 PCR 揭示了肺静脉异位连接的肺泡毛细血管发育不良家族中存在低水平的 FOXF1 体体细胞嵌合现象。
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A novel mutation in FOXF1 gene associated with alveolar capillary dysplasia with misalignment of pulmonary veins, intestinal malrotation and annular pancreas.与肺静脉异位连接、肠旋转不良和环状胰腺相关的 FOXF1 基因突变。
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Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.16号染色体长臂24.1区域FOX基因簇的基因组和基因缺失以及FOXF1的失活突变会导致肺泡毛细血管发育异常和其他畸形。
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