Laparoscopic Management of Persistent Müllerian Duct Syndrome

Abstract

Persistent Mullerian duct syndrome (PMDS) is characterized by persistence of Mullerian derivatives in a phenotypically and genotypically normal male. These patients have 46 XY karyotype with normal male external genitalia, virilization, and internal Mullerian duct structures. Typically, these patients have unilateral or bilateral undescended testes, bilateral fallopian tubes, a uterus, and an upper vagina draining into a prostatic utricle, as reported by Diamond and Uy (n.d.). We report a case of PMDS in a 25-year-old male, which present with primary infertility with bilateral cryptorchidism.