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

被引:9
|
作者
Ma, Youngeun [1 ]
Jang, Mi-Ae [3 ]
Yoo, Hye Soo [1 ]
Ahn, So Yoon [1 ]
Sung, Se In [1 ]
Chang, Yun Sil [1 ]
Ki, Chang-Seok [2 ]
Park, Won Soon [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, 81 Irwon Ro, Seoul 06351, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Lab Med & Genet, 81 Irwon Ro, Seoul 06351, South Korea
[3] Soonchunhyang Univ, Coll Med, Bucheon Hosp, Dept Lab Med & Genet, Bucheon, South Korea
关键词
Alveolar capillary dysplasia with misalignment of pulmonary veins; FOXF1; Korean; pathogenic; variant; TRANSCRIPTION FACTOR; VASCULATURE; LUNG;
D O I
10.3349/ymj.2017.58.3.672
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:672 / 675
页数:4
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