Recurrent Congenital Anterior Segment Dysgenesis: Identification of Pathogenic FOXE3 Gene Mutation and Its Implications for Future Pregnancies

Key Points

• Pathogenic mutations in the FOXE3 gene contribute to congenital anterior segment dysgenesis.
• Genetic analysis revealed a novel FOXE3 mutation affecting eye development.
• This analysis highlights the need for genetic counseling and testing in at-risk families.
• Findings may inform prenatal care and family planning for future pregnancies.