Abstract
Mullerian duct anomalies are infrequently encountered in day to day gynaecology practice. They result from defective fusion or defective absorption of female reproductive system during embryonic life. Though majority of patients with mullerian anomalies are asymptomatic, nearly one quarter may present with symptoms and signs of obstruction/reproductive dysfuntion. A rare pregnancy in a non-communicating rudimentary horn with rupture is presented.
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