Results 31 to 40 of about 4,325 (182)

Evaluation of Maternal and Foetal Outcome in Patients with Incidentally Diagnosed Müllerian Anomaly during Caesarean Section: A Retrospective Descriptive Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Introduction: Congenital uterine anomalies, also known as Müllerian anomalies, have an overall prevalence rate of 0.06% to 38%, depending on the type of study population and diagnostic techniques used in various studies.
Deepali Raina   +4 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome with borderline serous cystadenoma of the ovary: case report and literature review

open access: yesRadiology Case Reports, 2021
Herlyn-Werner-Wunderlich syndrome, is a rare urogenital congenital anomaly. Coexisting Mullerian ducts anomalies and ovarian neoplasms are rarely reported.
Johara AlMulhim, MD   +1 more
doaj   +1 more source

Unus pro omnibus, omnes pro uno: A novel, evidence-based, unifying theory for the pathogenesis of endometriosis [PDF]

open access: yes, 2017
The theory of retrograde menstruation as aetiopathogenesis of endometriosis formulated by John Sampson in 1927 shows clear shortcomings: this does not explain why retrograde menstruation is a physiological process that affects 90% of women, while ...
Acien   +203 more
core   +1 more source

Müllerian Anomalies: Revisited

open access: yesJournal of Gastrointestinal and Abdominal Radiology
The Müllerian structures are developed from paired embryologic ducts that undergo fusion and resorption in utero to form the uterus, fallopian tubes, cervix, and upper two-thirds of the vagina.
Tulika Singh   +3 more
doaj   +1 more source

Transverse testicular ectopia with disorders of sex development

open access: yesIndian Journal of Urology, 2012
Transverse testicular ectopia (TTE) is a rare congenital anomaly. Although TTE often coexists with abnormalities such as inguinal hernia and persistent Mullerian duct syndrome, disorders of sex development (DSD) in combination with TTE is extremely rare.
Katsuya Aoki   +3 more
doaj   +1 more source

A case of congenital unilateral partial absence of fallopian tube [PDF]

open access: yes, 2010
Congenital partial absence of a fallopian tube has rarely been reported in the literature. A 29-year-old nulligravida woman presented with a two-year history of infertility.
Endo, Sumiko   +7 more
core   +1 more source

A méhüreg anatómiai rendellenességei habituális vetélőkben [PDF]

open access: yes, 2015
Absztrakt Bevezetés: A habituális vetélés a nők 1%-át érintő rendellenesség, amelynek hátterében genetikai, endokrin, méhűri anatómiai, immunológiai, mikrobiológiai és hematológiai, valamint ...
Fekete, Dávid   +4 more
core   +1 more source

Complex mullerian duct anomaly in a young female with primary amenorrhoea, infertility, and chronic pelvic pain

open access: yesJournal of Human Reproductive Sciences, 2012
Mullerian duct anomalies, though rare, can be a treatable cause of pelvic pain and infertility. Various complex Mullerian duct anomalies may exist with combination of features of more than one class.
Sanyal Kumar   +2 more
doaj   +1 more source

Laparoscopic management of a cavitated noncommunicating rudimentary uterine horn of a unicornuate uterus: a case report

open access: yesJournal of Medical Case Reports, 2010
Introduction A unicornuate uterus with a rudimentary horn is the most uncommon uterine anomaly of the female genital tract. It has an estimated frequency of one in 100,000 among the fertile female population.
Perez-Medina Tirso   +3 more
doaj   +1 more source

A case of 20-week abortion in a rare communicating rudimentary horn of a misinterpreted unicornuate uterus, incorrectly diagnosed as bicornuate: A serious hazard! [PDF]

open access: yes, 2019
Female genital malformations, as the unicornuate uterus, are deviations from normal anatomy that could impair the reproductive potential of a woman or her health. We present a rare case of a 20-week spontaneous abortion in a 24 years old patient affected
Bifulco, Giuseppe   +7 more
core   +1 more source

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