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.
Cite
CITATION STYLE
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
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.