Abstract
Congenital Müllerian duct anomalies affect the female genital tract, including the fallopian tubes, uterus, cervix, and/or upper vagina. These anomalies occur due to agenesis or failed fusion of the paramesonephric ducts or failed resorption of the uterine septum during fetal development. The incidence of Müllerian duct anomalies ranges from 0.5% to 5.0% [1].Bicornuate uterus accounts for approximately one-fourth of these anomalies.
Siroliya A, Chouksey R. Bicornuate bicollis didelphic uterus with renal anomaly: pregnancy risks and complications [Internet]. South Asian J Case Rep Rev. 2025 [cited 2025 Sep 14];12(1):16-19. Available from: https://doi.org/10.18231/j.sajcrr.2025.005
APA
Siroliya, A., Chouksey, R. (2025). Bicornuate bicollis didelphic uterus with renal anomaly: pregnancy risks and complications. South Asian J Case Rep Rev, 12(1), 16-19. https://doi.org/10.18231/j.sajcrr.2025.005
MLA
Siroliya, Akanksha, Chouksey, Richa. "Bicornuate bicollis didelphic uterus with renal anomaly: pregnancy risks and complications." South Asian J Case Rep Rev, vol. 12, no. 1, 2025, pp. 16-19. https://doi.org/10.18231/j.sajcrr.2025.005
Chicago
Siroliya, A., Chouksey, R.. "Bicornuate bicollis didelphic uterus with renal anomaly: pregnancy risks and complications." South Asian J Case Rep Rev 12, no. 1 (2025): 16-19. https://doi.org/10.18231/j.sajcrr.2025.005