Abstract
Persistent Müllerian duct syndrome is a rare form of internal male pseudohermaphroditism caused by defects in synthesis or action of Müllerian-inhibiting factor, due to which Müllerian duct derivatives, such as uterus, fallopian tube, and upper vagina, are normally present in 46XY males. Here, we report a 26-year-old male with right-sided obstructed inguinal hernia with left undescended testis. On exploration, hernial sac containing bowel loops, uterus with fallopian tubes, upper vagina, and testes were present. © Association of Surgeons of India 2013.
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Patil, V., Muktinaini, S., Patil, R., & Verma, A. (2013). Persistent müllerian duct syndrome: A case report. Indian Journal of Surgery, 75(1 SUPPL.), 460–462. https://doi.org/10.1007/s12262-013-0831-6
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