Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome

Prenat Diagn. 2025 Dec;45(13):1799-1802. doi: 10.1002/pd.70019. Epub 2025 Nov 14.

Authors

Mia B Hodges¹, Kelly L Gilmore², Madeline J Dyke², Neeta L Vora²

Affiliations

¹ University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
² Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

No abstract available

Keywords: FGFR1; fetal genetic analysis; fetal imaging; hartsfield syndrome; prenatal diagnosis; whole genome sequencing.

Publication types

Case Reports

Grants and funding