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

Congenital Mullerian duct anomalies are conditions involving the female genital tract. Cases of complex Mullerian duct anomalies with involvement of the renal system are rare. Occasionally, these cases can be associated with obstetrical complications.

Uterine malformations are seen in about 7%-10% of women in the general population [1]. They result from either the abnormal formation or fusion of the para-mesonephric and mullerian ducts, or dissolution of the septum during embryonic life, resulting