Results 71 to 80 of about 1,504,083 (159)

An eventful journey from menarche to successful motherhood

open access: yesJournal of Human Reproductive Sciences, 2016
Herlyn–Werner–Wunderlich syndrome is an uncommon variant of mullerian duct anomaly and the approach to its diagnosis requires a high index of suspicion and vigilant work up. Presented here is a case of a 26yearold woman who had the aforementioned anomaly
Salil B Chakrabarti   +3 more
doaj   +1 more source

Complex Presentation of Uterus Didelphys With Bilateral Leiomyomas: A Case Report

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2025, Issue 1, 2025.
Müllerian duct anomalies and uterine leiomyomas represent distinctive facets of female reproductive health. While uterine leiomyomas are prevalent reproductive pathologies, the coexistence of Müllerian anomalies and leiomyomas is relatively uncommon. This case study examines the complex medical and surgical management of a woman who initially presented
Assaye Mezgebu Wube   +6 more
wiley   +1 more source

Herlyn-Werner-Wünderlich syndrome: case report

open access: yesCase Reports, 2018
Introduction: The Herlyn-Werner-Wünderlich (HWW) syndrome is the association of three urogenital anatomic alterations of low incidence. Müllerian alterations are rare and are usually incidental findings; consequently, they are underdiagnosed and their ...
Andrés Felipe Figueroa-Blanco   +1 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome in a adolescent girl

open access: yesLiječnički vjesnik, 2023
Herlyn-WernerWunderlich syndrome (HWWS) is a rare congenital genitourinary anomaly with uterine anomalies, unilateral cervicovaginal obstruction, and ipsilateral renal anomalies resulting from the embryological arrest of Müllerian and mesonephric ducts ...
Vita Jugovac   +4 more
doaj   +1 more source

Assessing the true prevalence of endometriosis: A narrative review of literature data

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 167, Issue 3, Page 883-900, December 2024.
Abstract Endometriosis is a gynecologic condition often described as the “chameleon of gynecology” because of its elusive symptoms. The World Health Organization acknowledges its severe impact on quality of life due to pain, fatigue, depression, and infertility.
Carolin Harder   +4 more
wiley   +1 more source

Herlyn-Werner-Wunderlich syndrome: a rare cause of infertility (2009: 2b)

open access: yes, 2009
Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis is a rare and specific entity referred to as Herlyn-Werner-Wunderlich syndrome.
Demir, Mustafa Kemal, Sarac, Armagan
core   +1 more source

Herlyn-Werner-Wunderlich syndrome: An "early" onset case report and review of Literature [PDF]

open access: yes, 2015
Herlyn-Werner-Wunderlich syndrome (HWWS) is a rare congenital mullerian anomaly consisting of uterus didelphys, hemivaginal septum, and unilateral renal agenesis [1,2].
Sica, M.   +10 more
core   +2 more sources

Vaginoscopic resection of hemivagina, in a 20‐year‐old virgin female with prior misdiagnosis of OHVIRA syndrome as a bicornuate uterus: A case report

open access: yesClinical Case Reports, Volume 12, Issue 3, March 2024.
Key Clinical Message OHVIRA syndrome can be misdiagnosed due to its rarity, resulting in the need for more invasive interventions than vaginoscopy. Also, delayed diagnosis of OHVIRA syndrome can affect patient's quality of life by leading to chronic gynecological diseases such as endometriosis and pelvic inflammatory disease.
Ameneh Haghgoo   +3 more
wiley   +1 more source

A rare case of Herlyn-Werner-Wunderlich syndrome-with pregnancy

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2016
Herlyn-Werner-Wunderlich syndrome also known as uterus didelphys with obstructing hemivaginal septum and ipsilateral renal agenesis (OHVIRA) is a very rare syndrome with only a few case reported.
Vikas Deswal   +3 more
doaj   +1 more source

Zinner Syndrome: The Diagnosis and Management of a Rare Urogenital Malformation

open access: yesCase Reports in Radiology, Volume 2024, Issue 1, 2024.
This case highlights an atypical but important consideration in young males presenting with persistent gastrointestinal and/or genitourinary symptoms. Zinner syndrome (ZS) develops from embryologic maldevelopment of the distal mesonephric duct, resulting in ejaculatory duct atresia with consequent obstruction of the seminal vesicle and concomitant ...
Lucinda Lau   +5 more
wiley   +1 more source

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