Abstract
Abstract Uterine didelphys results from impaired fusion of the paired Mullerian ducts. The incidence of uterine anomalies is believed to be 0.5–2.0% of reproductive-age women, with didelphic uterus accounting for approximately 10%. Uterine didelphys is associated with renal agenesis in approximately 25% of cases. We present a case of didelphys uterus with a left solitary kidney in a mother whose female fetus also demonstrated uterine didelphys with right multicystic dysplastic kidney. This report highlights the significant contribution and complimentary role of fetal MRI in identifying fetal anomalies.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
