P823: Genetics of fetal micrognathia: One fetal center’s experience
Fetal micrognathia is a common craniofacial abnormality, affecting around 1/1,500 births. There are multiple genetic syndromes known to cause micrognathia with variable neonatal outcomes. In some cases, micrognathia is seen as an isolated finding with or without a family history. Therefore, it becomes difficult to counsel families on the potential outcomes they may expect for their child. The aim of this research is to better understand the genetic contribution of prenatal micrognathia.
Authors
- Natalie Burrill (ORCID: https://orcid.org/0000-0002-6046-5999)
- K. Taylor Wild (ORCID: https://orcid.org/0000-0002-0016-078X)
- Lisa Pilchman
- William H. Peranteau (ORCID: https://orcid.org/0000-0003-1608-861X)
- Juliana S. Gebb (ORCID: https://orcid.org/0000-0001-5829-1961)
- Erica Schindewolf
- Edward Oliver (ORCID: https://orcid.org/0009-0000-7958-7016)
Institutions
- Children's Hospital of Philadelphia (US)
Publication Details
- Journal
- Genetics in Medicine Open
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1016/j.gimo.2025.103192
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00