Pathogenic variant in GATA4 associated with atrioventricular septal defect and congenital diaphragmatic hernia: A case report
Pathogenic variants in GATA4, a transcription factor, are predominantly associated with congenital heart defects and gonadal abnormalities. We describe a case of a maternally inherited GATA4 pathogenic variant (c.474C > G p.[Tyr158Ter]) in a 21-week gestation fetus presenting with partial atrioventricular septal defect and congenital diaphragmatic hernia. Whilst there is a weight of evidence implicating GATA4 dysfunction in congenital diaphragmatic hernia, this is only the second report to our knowledge to identify a causative GATA4 variant with congenital diaphragmatic hernia.
Authors
- Aris T. Papageorghiou (ORCID: https://orcid.org/0000-0001-8143-2232)
- Trisha V. Vigneswaran (ORCID: https://orcid.org/0000-0002-4084-4203)
- John Howat (ORCID: https://orcid.org/0009-0007-5844-4375)
- Sahar Mansour (ORCID: https://orcid.org/0000-0001-8357-1287)
Institutions
- St George’s University Hospitals NHS Foundation Trust (GB)
- St George's Hospital (GB)
- Evelina London Children's Healthcare (GB)
Publication Details
- Journal
- European Journal of Medical Genetics
- Published
- 2025-11-10
- DOI
- https://doi.org/10.1016/j.ejmg.2025.105059
- Primary Topic
- Congenital heart defects research
- Type
- article
- Field-Weighted Citation Impact
- 0.00