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Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next‐generation sequencing
Author(s) -
Kammoun Molka,
Souche Erika,
Brady Paul,
Ding Jia,
Cosemans Nele,
Gratacos Eduard,
Devriendt Koen,
Eixarch Elisenda,
Deprest Jan,
Vermeesch Joris Robert
Publication year - 2018
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.5327
Subject(s) - congenital diaphragmatic hernia , candidate gene , genetics , biology , genotype , phenotype , gene , medicine , fetus , pregnancy
Background Congenital diaphragmatic hernia (CDH) is characterized by a defective closure of the diaphragm occurring as an isolated defect in 60% of cases. Lung size, liver herniation, and pulmonary circulation are major prognostic indices. Isolated CDH genetics is heterogeneous and poorly understood. Whether genetic lesions are also outcome determinants has never been explored. Objectives To identify isolated CDH genetic causes, to fine map the mutational burden, and to search for a correlation between the genotype and the disease severity and outcome. Methods Targeted massively parallel sequencing of 143 human and mouse CDH causative and candidate genes in a cohort of 120 fetuses with isolated CDH and detailed outcome measures. Results Pathogenic and likely pathogenic variants were identified in 10% of the cohort. These variants affect both known CDH causative genes, namely, ZFPM2 , GATA4 , and NR2F2 , and new genes, namely, TBX1 , TBX5 , GATA5 , and PBX1 . In addition, mutation burden analysis identified LBR , CTBP2 , NSD1 , MMP14 , MYOD1 , and EYA1 as candidate genes with enrichment in rare but predicted deleterious variants. No obvious correlation between the genotype and the phenotype or short‐term outcome has been found. Conclusion Targeted resequencing identifies a genetic cause in 10% of isolated CDH and identifies new candidate genes.