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International Journal of Recent Trends in Science and Technology, ISSN 2277-2812 E-ISSN: 2249-8109

Volume 12, Issue 3, September 2014 pp 505-506

Case Report

A rare case of uterine didelphys

Sudha R1, Sunanda N2, Babitha M C3

1Associate Professor, 2Assisant Professor, 3Postgraduate, Department of OBGY, MMCRI, Mysore, Karnataka, INDIA.


Uterus didelphys is one of the congenital uterine anomalies due to defective medial fusion of Mullerian ducts. Often remains asymptomatic and hence undetected. Women with congenital uterine alformation usually have higher incidence of complications during pregnancy and delivery. Although pregnancies can occur in patients with Mullerian duct anomalies, most of them have been linked to infertility, recurrent pregnancy loss, pre term deliveries, fetal mal-presentations and other obstetrics complications, making successful pregnancy outcome a rare situation in this condition. We report a case of successful pregnancy outcome in a case of uterus didelphys bicollis. A 25year old P2L2 with 2 previous LSCS, failed LS, with 2 months of amenorrhea, continued her pregnancy till term and underwent cesarean section with concurrent sterilization.