EAS Publisher | Pregnancy Follow Up and Delivery of Didelphys Uterus: Case Report and Review of Literature

Pregnancy Follow Up and Delivery of Didelphys Uterus: Case Report and Review of Literature

DOI : https://doi.org/10.36349/easjms.2025.v07i11.005

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DEAR EDITOR Congenital uterine anomalies arise from abnormal embryological development of the paramesonephric ducts (or Mullerian ducts) [1]. Various anomalies result from arrested development of the uterovaginal primordium during embryonic period, by incomplete or failed development of parts of one or both paramesonephric duct, incomplete fusion of the paramesonephric ducts or incomplete canalization of the vaginal plate [2]. Prevalence of all types of female congenital reproductive tract malformations is estimated at 4%–7% and they are mostly benign [3]. Uterine didelphys is a rare type of anomaly with estimated prevalence of 0.3%, caused by complete failure of fusion of the inferior parts of the paramesonephric ducts resulting in separate uterine cavities with two cervices and a double or single vagina. Sometimes a longitudinal or transverse vaginal septum varying from thin and easily displaceable to thick and inelastic may also

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