This report addresses and discusses two cases of uterine didelphys in pregnancy. The first case describes the diagnosis, management and subsequent pregnancies in a 28-year-old woman, para 2, with known didelphys uterus, left-obstructed hemi-vagina and

Congenital malformations of the uterus are the consequence of an anomaly in combination, canalization, and resorption of the septum during the development of Mullerian ducts. Buttram and Gibbons initially classified Mullerian duct anomalies depending

Background. Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. A didelphys uterus, also known as a “double uterus,” is one of the least common