RARE CASE REPORTS OF COMPLETE UTERINE SEPTUM WITH LONGITUDINAL VAGINAL SEPTUM PRESENTING AS DIDELPHIC/ UNICORNUATE UTERUS

Journal Title: Journal of Evolution of Medical and Dental Sciences - Year 2017, Vol 6, Issue 94

Abstract

PRESENTATION OF CASE Müllerian duct anomalies (MDA) comprise of a heterogeneous group of genital malformations accounting for an incidence of 3% - 4% in the general female population. Use of improved imaging modalities such as 3D transvaginal ultrasound (TVUS) and magnetic resonance imaging (MRI) has helped clinicians to better identify and characterise such anomalies.[1] Septate uterus with cervical duplication and longitudinal vaginal septum is a rare Müllerian anomaly, hence its true incidence is not known. We report 2 cases of this rare anomaly.

Authors and Affiliations

Kalpana B, Richa Gupta

Keywords

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  • EP ID EP279997
  • DOI 10.14260/jemds/2017/1501
  • Views 73
  • Downloads 0

How To Cite

Kalpana B, Richa Gupta (2017). RARE CASE REPORTS OF COMPLETE UTERINE SEPTUM WITH LONGITUDINAL VAGINAL SEPTUM PRESENTING AS DIDELPHIC/ UNICORNUATE UTERUS. Journal of Evolution of Medical and Dental Sciences, 6(94), 6920-6922. https://europub.co.uk./articles/-A-279997