Results 11 to 20 of about 625 (137)

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
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 ...
Ameneh Haghgoo   +3 more
doaj   +2 more sources

Diagnosis and surgical treatment of obstructed hemivagina and ipsilateral renal anomaly in a dog: a case report [PDF]

open access: yesFrontiers in Veterinary Science
Obstructed hemivagina and ipsilateral renal agenesis (OHVIRA), also called Herlyn–Werner–Wunderlich syndrome, is an extremely rare Müllerian duct anomaly accompanied by Wolffian duct anomalies.
Younwoo Choo   +5 more
doaj   +2 more sources

Magnetic Resonance Imaging Evaluation of Wolffian Duct Anomalies – OHVIRA and OSVIRA [PDF]

open access: yesJournal of Human Reproductive Sciences
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.
Lukshay Bansal   +2 more
doaj   +2 more sources

Síndrome de OHVIRA, a propósito de un caso

open access: yesUniversidad y Salud, 2020
Introducción: El síndrome de obstrucción hemivaginal y anomalía renal ipsilateral (OHVIRA, por sus siglas en inglés) o también llamado síndrome de Herlyn-Werner-Wunderlich es una rara malformación mulleriana que consiste en la presencia de útero didelfo,
John Jamer Paz-Montañez   +2 more
doaj   +3 more sources

Case Series of Reproductive Outcomes after Surgical Correction of Obstructed Hemivagina in OHVIRA [PDF]

open access: yesAmerican Journal of Perinatology Reports
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) is a rare congenital developmental syndrome manifested by uterine duplication, lower genital tract obstruction, and unilateral renal anomaly. Literature on reproductive outcomes in this patient
Megan E. Bunnell   +2 more
doaj   +2 more sources

OHVIRA and OSVIRA syndrome [PDF]

open access: yesIndian Journal of Radiology and Imaging, 2018
Raj Bharatkumar Koticha
doaj   +3 more sources

A non-classic presentation of OHVIRA syndrome

open access: yesPortuguese Journal of Pediatrics
A 13-year-old female adolescent was admitted to the Pediatric Emergency Department with abdominal pain and occasional vomiting, for three days.
Filipa da Costa-Cascais   +3 more
doaj   +2 more sources

Clinical features and surgical options of obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome: A systematic review and a meta-analysis of prevalence. [PDF]

open access: yesInt J Gynaecol Obstet
Abstract Background OHVIRA syndrome, a urogenital malformation, lacks standardized management. Narrative reviews exist, but there is no a comprehensive meta‐analysis. Objectives The aim of this first systematic review and meta‐analysis is to evaluate the current literature and inform management strategies.
Bonetti E   +8 more
europepmc   +2 more sources

The Herlyn-Werner-Wunderlich Syndrome: a Rare Case Report [PDF]

open access: yesJournal of Liaquat National Hospital, 2023
Obstructed Hemivagina and Ipsilateral Renal Agenesis (OHVIRA) is an aberrated and special type of Mesonephric duct malformation and Müllerian duct anomaly. This mostly reports 5% of Müllerian duct anomalies. The majority of cases of OHVIRA are presented
Uzma Panhwer   +4 more
doaj   +1 more source

Retroperitoneal teratoma with obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome in infant

open access: yesJournal of Pediatric Surgery Case Reports, 2021
The reports of retroperitoneal teratoma or obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome were published respectively. But there were no reports of retroperitoneal teratoma with OHVIRA syndrome.
Tamaki Iwade, Koichi Ohno
doaj   +1 more source

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