Ultrasound Diagnosis of Mayer-Rokitansky-Küster-Hauser Syndrome in a Resource-Limited Setting: A Case Report from Nigeria

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Shakirah G. AbdulAzeez
Jessica C. Akonobi
Musa Y. Dambele

Abstract

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital Müllerian anomaly and an important cause of primary amenorrhea. We report a 27-year-old Nigerian woman with normal secondary sexual characteristics. Transabdominal pelvic ultrasound showed complete uterine agenesis, with normal bilateral ovaries and kidneys, consistent with type I MRKH syndrome. This case demonstrates that ultrasound can provide a reliable, accessible, and affordable diagnosis in resource-limited settings where magnetic resonance imaging is unavailable or unaffordable, enabling timely counseling, psychological support, and multidisciplinary management.

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Author Biographies

Shakirah G. AbdulAzeez, Osun State University, Osogbo, Osun State

Department of Radiography and Radiation Sciences, Faculty of Basic Medical Science

 

Jessica C. Akonobi, Osun State University, Osogbo, Osun State

Department of Radiography and Radiation Science, Faculty of Basic Medical science

Musa Y. Dambele, Bayero University, Kano

Department of Medical Radiography, Faculty of Allied Health Sciences

How to Cite

AbdulAzeez, S. G., Akonobi, J. C., & Dambele, M. Y. (2026). Ultrasound Diagnosis of Mayer-Rokitansky-Küster-Hauser Syndrome in a Resource-Limited Setting: A Case Report from Nigeria. Journal of Radiography and Radiation Sciences, 40(1), 10-13. https://doi.org/10.82547/jrrs/2026/IAPK3355

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