The retrospective data analysis of NLRP7 and KHDC3L mutations in Turkish patients with recurrent hydatidiform mole

Objective: gene mutations in our Turkish cohort with recurrent molar pregnancies, and to establish genotype-phenotype correlation. Materials and Methods: sequencing. Results: gene variants were first reported in this study. Conclusion: mutations. The current study highlights the importance of defining new cases and novel mutations in the pathogenesis and clinical management of RHM. Understanding genotype-phenotype correlations in RHM patients will also contribute to the selection of treatment methods and patient management.