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A 35-year-old father with persistent Mullerian duct syndrome and seminoma of the right undescended testis: a rare case report [PDF]

open access: yesSurgical Case Reports, 2021
Background A persistent Müllerian duct syndrome is a rare disorder of sexual differentiation characterized by the presence of the female reproductive system in a normal male.
Marah Mansour   +4 more
doaj   +3 more sources

Persistent Mullerian duct syndrome [PDF]

open access: yesUrology Case Reports
Persistent Müllerian Duct Syndrome is a rare genetic disorder, consisting in the persistence of the müllerian structures in males. We report the case of a 29-year-old male patient presented with an abdominopelvic mass.
Ons Krimi   +7 more
doaj   +2 more sources

Persistent Mullerian Duct Syndrome in an Adult Infertile Male: A Case Report [PDF]

open access: yesJournal of Nepal Medical Association
Persistent Müllerian duct syndrome is a rare autosomal recessive disorder of sex development characterized by the presence of Müllerian duct derived structures in a normally virilized, genotypical (46, XY) and phenotypical male.
Nesuma Sedhain   +3 more
doaj   +2 more sources

Persistent Müllerian Duct Syndrome: Understanding the Challenges [PDF]

open access: yesCase Reports in Urology, 2022
Persistent Müllerian duct syndrome (PMDS) is a rare autosomal recessive condition defined by the presence of Müllerian duct-derived structures in an otherwise normally masculinized phenotypical and genotypical (46,XY) male.
Irene Chua, Naeem Samnakay
doaj   +2 more sources

Prostatic adenocarcinoma in a patient with persistent Müllerian duct syndrome [PDF]

open access: yesUrology Annals, 2022
The embryonal male sexual differentiation is driven by testosterone, and Anti-Müllerian hormone (AMH). AMH is responsible for regression of Müllerian ducts in a genetically male fetus.
Muhammad Umair   +7 more
doaj   +2 more sources

Transverse testicular ectopia with persistent mullerian duct syndrome: Misdiagnosis and surgeon's unexpected discovery: A case report [PDF]

open access: yesUrology Case Reports, 2022
Reports on the occurrence of persistent mullerian duct syndrome along with transverse testicular ectopia are extremely rare globally. In this condition, the fallopian tubes, uterus, cervix and upper two-thirds of vagina occurs alongside transverse ...
Najib Isse Dirie   +4 more
doaj   +2 more sources

Fortuitous Persistent Müllerian Duct Syndrome Diagnosis in an Adult Patient With Hematuria: A Case Report [PDF]

open access: yesClinical Case Reports
Persistent Müllerian duct syndrome is a genetic disorder. It consists of Müllerian duct remains due to improper anti‐Müllerian hormone. Early life presentation is often associated with undescended testes or inguinal hernias.
Alexi Boitsios   +3 more
doaj   +2 more sources

Management of Groin Pain Using an Iliohypogastric Nerve Block in a Patient with Inguinal Hernia due to Persistent Müllerian Duct Syndrome [PDF]

open access: yesCase Reports in Urology, 2021
Persistent Müllerian duct syndrome can cause an inguinal hernia, although this is a rare occurrence; recurrent inguinal hernias can, in turn, cause ongoing groin pain. Management of groin pain plays an important role in patients’ quality of life.
Takanori Sekito   +5 more
doaj   +2 more sources

Cancer on cryptorchid testis revealing a Persistent Müllerian Duct Syndrome: A rare case [PDF]

open access: yesUrology Case Reports, 2019
The persistence of Müllerian derivatives syndrome or PDMS is a rare form of male pseudohermaphrodism. Its association to ectopic testicular cancer is even rarer. Because of its rarity it is difficult to diagnose preoperatively.
Ahmed Samet   +5 more
doaj   +2 more sources

Blood in semen as a clue [PDF]

open access: yesRevista de la Facultad de Ciencias Médicas de Córdoba
A 21-year-old man presented with blood in his semen and was diagnosed with Persistent Müllerian Duct Syndrome (PMDS). This rare genetic condition occurs due to insufficient Anti-Müllerian Hormone (AMH) production or AMH insensitivity, resulting in the ...
Jheniffer Cação   +3 more
doaj   +2 more sources

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