International Journal For Multidisciplinary Research

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A Widely Indexed Open Access Peer Reviewed Multidisciplinary Bi-monthly Scholarly International Journal

Call for Paper Volume 7, Issue 3 (May-June 2025) Submit your research before last 3 days of June to publish your research paper in the issue of May-June.

Case Presentation of Congenital Anomaly of Uterus: Short Review of A Case

Author(s) Birjis Fatma, Dr. Abid Nadeem Nomani, Prof. Suboohi Mustafas, Dr. Muhammed Nadeem Khan
Country India
Abstract Müllerian duct anomalies are congenital abnormalities of the female reproductive system. (MDAs) are caused by aberrant Müllerian duct formation during embryonic development. A unicornuate uterus arises when one of the paired Müllerian ducts fails to mature or union, whose primordial horn may or may not be present. Preterm birth, intrauterine foetal demise, and spontaneous miscarriage are among the obstetric difficulties that women with this illness are more likely to experience. They might also suffer from gynaecological problems like endometriosis, infertility, and painful periods. A 14-year-old single girl arrived at the Niswan-Wa-Qabalat OPD of Ajmal Khan Tibbiya College, Aligarh Muslim University, complaining of lower abdominal pain and no menstruation throughout a single menstrual cycle. A complete medical history, examination, and imaging modality, such as ultrasound, indicating the patient has a right unicornuate uterus and a left rudimentary non-cavitated uterine horn.
In conclusion, a young, healthy-looking adolescent girl's lack of a regular menstrual cycle should raise suspicions of a unicornuate uterus because it may impact her future ability to conceive. The patient should receive appropriate counselling in addition to a variety of treatment options, including non-surgical and surgical treatments.
Keywords congenital anomaly of uterus, unicornuate uterus, American Fertility Society
Field Medical / Pharmacy
Published In Volume 7, Issue 3, May-June 2025
Published On 2025-05-27
DOI https://doi.org/10.36948/ijfmr.2025.v07i03.45994
Short DOI https://doi.org/g9mn3f

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