Results 31 to 40 of about 1,764,956 (149)

Reviewing recherche presentations of persistent Mullerian duct syndrome: case reports

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2022
Background Persistent Mullerian Duct Syndrome (PMDS) is a type of pseudo-hermaphroditism occurring in males internally due to failure in the Anti Mullerian Hormone (AMH)-dependent sex differentiation pathway.
Aishwarya Jeyakumar   +4 more
doaj   +1 more source

Persistant Mullerian duct syndrome with intra-abdominal seminoma

open access: yesUrology Case Reports, 2020
Persistent Mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism; it is defined by the presence of the Mullerian duct derivatives (the uterus, the fallopian tubes, and the upper vagina) in genotypically and phenotypically males ...
Ali Al-Asmar   +5 more
doaj   +1 more source

Robot-assisted hysterectomy in a 41-year-old male: A rare case report

open access: yesUrology Case Reports, 2020
Persistent Müllerian Duct Syndrome (PMDS) is regarded as a rare genetic disorder influencing internal sexual male development. PMDS is commonly diagnosed incidentally either during any pelvic surgery or examination of undescended testis.
Saud Almousa   +5 more
doaj   +1 more source

Persistent Mullerian duct syndrome and bilateral cryptorchidism

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Introduction: persistent Müllerian duct syndrome (PMDS) is a rare condition occasionally encountered in men with normal phenotype but with influencing internal sexual male development. This disorder is characterized by the presence of female reproductive
Marjan Joudi   +4 more
doaj   +1 more source

Management of a rare case: transverse testicular ectopia associated with persistent mullerian duct syndrome [PDF]

open access: yes, 2021
Transverse testicular ectopia (TTE) is a rare congenital anomaly in boys, which is characterized by the migrate of both testicles towards the same hemiscrotum or inguinal region.
Demirtaş, Mehmet Semih, Tuşat, Mustafa
core   +1 more source

Obstructed inguinal hernia in an adult male: A rare presentation of persistent Müllerian duct syndrome (internal male pseudohermaphroditism): A case report

open access: yesInternational Journal of Abdominal Wall and Hernia Surgery, 2022
Persistent Müllerian duct syndrome (PMDS) is an unusual form of internal male pseudohermaphroditism in which Müllerian duct derivatives are seen in phenotypically normal males, with 46, XY karyotype.
Musharraf Husain   +3 more
doaj   +1 more source

Decision-making in pediatric persistent Mullerian duct syndrome [PDF]

open access: yes, 2018
We are reporting a case of an 18-month old male who presented with bilateral cryptorchidism. The patient underwent an explorative laparoscopy in which two gonads were identified in close proximity to the uterus and fallopian tubes.
Shaltaf, Ahmad   +4 more
core   +1 more source

A Case Report of Patient Presenting with Huge Abdominal Seminoma and Persistent Mullerian Duct Syndrome

open access: yesHitit Medical Journal, 2021
Persistent Mullerian Duct Syndrome is a very rare form of male pseudo hermaphroditism. It is characterized by the presence of Mullerian duct derivatives (uterus, fallopian tubes and upper two-third of vagina) in genotypically and phenotypically normal ...
Nihan Turhan   +3 more
doaj  

Management of Transverse Testicular Ectopia with Persistent Mullerian Duct Syndrome

open access: yesİstanbul Kuzey Klinikleri, 2018
According to additional anomalies, transverse testicular ectopia (TTE) is classified into three groups. Type-2 TTE, accompanied by persistent mullerian duct syndrome, constitutes approximately 20% of the patients.
Sabri Cansaran   +4 more
doaj   +1 more source

Persistent Mϋllerian duct syndrome presenting as bilateral cryptorchidism: a case report

open access: yesAfrican Journal of Urology, 2022
Background Persistent Mϋllerian duct syndrome is a rare condition marked by the presence of Mϋllerian duct derivatives (uterus and fallopian tubes) in males who are seemingly (phenotypically and karyotypically) normal. Diagnosis can be made with physical
Mahesh Joshi   +3 more
doaj   +1 more source

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