Results 21 to 30 of about 114,600 (162)

Persistent Mullerian Duct Syndrome with Transverse Testicular Ectopia: Rare Entity [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
We are reporting on a 35-year-old male from low socio-economic strata, who presented with a left-sided inguinal hernia. Intraoperatively, a uterus and two fallopian tubes were found in the hernial sac which was adjacent to the two gonads, which received
Deepika, Abhay Kumar
doaj   +1 more source

Lhx1 is required in Müllerian duct epithelium for uterine development [PDF]

open access: yes, 2014
The female reproductive tract organs of mammals, including the oviducts, uterus, cervix and upper vagina, are derived from the Müllerian ducts, a pair of epithelial tubes that form within the mesonephroi.
Kwan, Kin Ming   +3 more
core   +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

Complete Müllerian agenesis, renal agenesis, and renal ectopia: MURCS association – A rare cause of primary amenorrhea

open access: yesApollo Medicine, 2019
Müllerian duct aplasia–renal agenesis–cervicothoracic somite dysplasia (MURCS) association is a rare and unusual constellation of nonrandom findings that include Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia. The agenesis of
Reddy Ravikanth, Pooja Majumdar
doaj   +1 more source

Complete Uterine Septum with Duplicate Cervix, Longitudinal Vaginal Septum and Unilateral Vaginal Obstruction (Herlyn-Werner-Wunderlich Syndrome): A Case Report of a Mullerian Duct Anomaly [PDF]

open access: yesWomen’s Health Bulletin, 2021
Introduction:Herlyn-Werner-Wunderlich Syndrome (HWWs) is a rare variant of Mullerian duct anomalies. It is associated with a wide range of gynecological and obstetric complications, such as urinary incontinence, urinary retention, endometriosis, pelvic ...
Leili Hafizi   +2 more
doaj   +1 more source

Embryological basis of malformed female genital tract and various classifications

open access: yesNational Journal of Clinical Anatomy, 2014
Developmental anomalies of the Mullerian duct system represent some of the most fascinating disorders that obstetricians and gynaecologists encounter.
Richa Niranjan, A K Singh, Anjoo Yadav
doaj   +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

The cell biology and molecular genetics of Müllerian duct development [PDF]

open access: yes, 2018
The Müllerian ducts are part of the embryonic urogenital system. They give rise to mature structures that serve a critical function in the transport and development of the oocyte and/or embryo.
Roly, ZY   +7 more
core   +1 more source

Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases

open access: yesIndian Journal of Urology, 2011
Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male.
Renuka V Inuganti   +3 more
doaj   +1 more source

Persistent mullerian duct syndrome

open access: yesIndian Journal of Radiology and Imaging, 2010
Persistent Mullerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism in which Mullerian duct derivatives are seen in a male patient. This syndrome is characterized by the persistence of Mullerian duct derivatives (i.e.
Divya Renu, B Ganesh Rao, K Ranganath
doaj   +3 more sources

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