Ohvira syndrome – a case report
Back ground: OHVIRA syndrome is a very rare congenital Uro-genital anomaly associated with both the Mullerian (paramesonephric) and Wolffian (mesonephric) systems. It is characterized by a triad, OHV – Obstructed Hemi vagina, IRA—Ipsilateral Renal Agenesis with associated uterus didelphs. Mullerian Duct anomalies 0.8-4% of the women who came for evaluation of infertility. OHVIRA syndrome-0.1-3.5% of the Mullerian Duct Anamoly. Aims: To discuss and analyse the radiological and embryological co-relation in OHVIRA syndrome and study the genesis of both the urinary and genital systems.