Zobrazeno 1 - 10
of 428
pro vyhledávání: '"ipsilateral renal agenesis"'
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 55, Iss 1, Pp 1-8 (2024)
Abstract Background Herlyn–Werner–Wunderlich syndrome also known as OHVIRA syndrome is a rare complex congenital developmental anomaly characterized by the triad of uterine didelphys, obstructed hemivagina causing hematometrocolpos and ipsilatera
Externí odkaz:
https://doaj.org/article/d562bc89410745efa64180e2e25483dc
Publikováno v:
Journal of Human Reproductive Sciences, Vol 17, Iss 2, Pp 128-132 (2024)
Herlyn–Werner–Wunderlich syndrome in females, also known as obstructed haemivagina and ipsilateral renal agenesis (OHVIRA), and Zinner’s syndrome, also known as OSVIRA in males, are two rare congenital syndromes affecting the urogenital tract.
Externí odkaz:
https://doaj.org/article/83e3f5ef665944838d91f05f8bcb0d46
Autor:
Prajwal Dahal, MD, Ongden Yonjen Tamang, MD, Rudra Prasad Upadhyaya, MD, Kapil Dawadi, MD, Prajina Pradhan, MD, Sabina Parajuli, MBBS
Publikováno v:
Radiology Case Reports, Vol 19, Iss 1, Pp 82-88 (2024)
Herlyn-Werner-Wunderlich (HWW) syndrome, popularly known by acronym of obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) is a rare Müllerian and Wolffian duct anomaly. The syndrome is classically described as triad of uterine didelphy,
Externí odkaz:
https://doaj.org/article/32fb7828eb4045cca2f131dda3f16be2
Autor:
Graziella Moufawad, Andrea Giannini, Ottavia D'Oria, Antonio Simone Laganà, Vito Chiantera, Aline Khazzaka, Ghida Maziad, Elena Nasr, Vanessa Geagea, Marwa Al Jardali, Zaki Sleiman
Publikováno v:
Gynecology and Minimally Invasive Therapy, Vol 12, Iss 3, Pp 123-129 (2023)
Obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome is a rare congenital defect of the Müllerian ducts characterized by uterus didelphys, unilateral obstructed hemivagina, and ipsilateral renal agenesis. The aim of this systematic
Externí odkaz:
https://doaj.org/article/ecbf0ad0397743fd9869df06855f1d07
Autor:
Faiz Manzar Ansari, MS, Sajad Ahmad Para, MS, MCh, Shashank Singh, MS, Mohammad Saleem Wani, MS, MCh, Arif Hamid Bhat, MS, MCh, Manjul Kumar Maurya, MS
Publikováno v:
Radiology Case Reports, Vol 18, Iss 1, Pp 131-134 (2023)
Zinner's syndrome is a rare developmental anomaly of Wolffian duct, comprising a triad of seminal vesicle cyst, ipsilateral renal agenesis and ejaculatory duct obstruction, first described by Zinner in 1914. Several aberrations have been reported lik
Externí odkaz:
https://doaj.org/article/6030ac14b2ad4139b30bddb1e046b3a8
Publikováno v:
Surgeries, Vol 4, Iss 1, Pp 10-16 (2022)
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare variant of mullerian duct anomalies characterized by the triad of uterine didelphys, obstructed hemivagina and ipsilateral renal agenesis. We report two cases of HWW syndrome in young women with abdom
Externí odkaz:
https://doaj.org/article/711a37d83bfd4da1850759a6340da817
Akademický článek
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Autor:
Lila H. Abu-Hilal, Duha I. Barghouthi, Yumna Njoum, Amal Obeid, Khaled Alshawwa, Tawfiq AbuKeshek, Mohammed Maree
Publikováno v:
Frontiers in Urology, Vol 3 (2023)
IntroductionZinner syndrome (ZS) is a rare condition characterized by a triad of seminal vesicle cyst (SVC), ipsilateral ejaculatory duct obstruction, and ipsilateral renal agenesis. The diagnosis is often delayed due to non-specific symptoms, such a
Externí odkaz:
https://doaj.org/article/a262f17b6a8e4c1dac35257d7571cbd2
Publikováno v:
Fertility & Reproduction, Vol 3, Iss 1, Pp 2-9 (2021)
The Herlyn–Werner–Wunderlich (HWW) syndrome is an uncommon Mullerian duct anomaly composed of a triad of obstructed hemivagina, renal agenesis, uterine didelphys with a prevalence of
Externí odkaz:
https://doaj.org/article/433b6d786efd47d69645a8851b352686
Publikováno v:
Medicina, Vol 59, Iss 4, p 703 (2023)
Background: Obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome, also known as Herlyn-Werner-Wunderlich syndrome, is a rare syndrome characterized by the triad of uterus didelphys, obstructed hemivagina, and ipsilateral renal agene
Externí odkaz:
https://doaj.org/article/e9bc3a219d674a19aba6ddb2f09ebcd6