Herlyn-Werner-Wunderlich (HWW) syndrome is a rare variant of mullerian duct anomalies characterized by the triad uterine didelphys, obstructed hemivagina and ipsilateral renal agenesis. We report two cases HWW in young women with abdominal pain. This diagnosis can easily be missed if clinician not aware syndrome. In one case, computed tomography image hematocolpos was initially mistaken for cys...

An eighteen month old phenotypically and genotypically normal male child was admitted with a left inguinal hernia and a right undescended testis. At operation, he was found to have a uterus, bilateral fallopian tubes, and a vagina in the left hernial sac. Bilateral orchidopexies and excision of the persistent Mullerian duct structures were carried out. This rare case of persistent Mullerian duc...

The paper focuses on anatomical varieties of developmental anomalies of female vagina’s outlet, emphasizing the role of their early recognition in preventing retrograde menstruation by surgical treatment at the beginning of puberty. Three different types of vaginal outlet obstruction are described: imperforate hymen from the group of hymen misdevelopment, transversal vaginal septum from the gro...

Complete bicornuate uterus is a type of Mullerian duct deformity, resulting from abnormal duct fusion. Similar to other Mullerian anomalies, bicornuate uterus is associated with specific complications during possible pregnancies. While various studies have reported successful deliveries in a bicornuate uterus, it might be accompanied with various complications, ranging from preterm labor to mor...

Introduction: Congenital uterine anomalies are common but their effect on reproductive outcome is unclear. result from abnormal formation, fusion or resorption of mullerian ducts during fetal life. The overall frequency 4%. In general fertile population the 5%, in infertile 3%. Recurrent miscarriages occur 5-10% cases. Materials and methods:A hospital based cross-sectional analytical study was ...