Persistent Mullerian duct syndrome: A rare cause of unilateral cryptorchidism

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Abstract

Persistent Mullerian duct syndrome (PMDS) is a rare syndrome and sometimes the cause of a common problem in paediatric and surgical practice, namely undescended testes. PMDS is a recessive disease in which there is a defect in anti-Mullerian hormone secretion or receptor activity resulting in persistence of Mullerian structures such as a uterus or fallopian tubes with otherwise normal virilisation. Here the authors present a case of a 1 1/2-year-old boy who was referred to their hospital because of unilateral cryptorchidism. During laparoscopic surgery, two gonads were present joined together by a uterus-like structure. Additional investigations showed a normal male karyotype and biopsies of the gonads revealed infantile testis parenchyma making the diagnosis PMDS likely. Copyright 2012 BMJ Publishing Group. All rights reserved.

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Keukens, L., Zijp, G., & Mul, D. (2012). Persistent Mullerian duct syndrome: A rare cause of unilateral cryptorchidism. BMJ Case Reports. https://doi.org/10.1136/bcr.02.2012.5722

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