Results 41 to 50 of about 1,735 (192)

Atypical presentation of obstructed hemivagina and ipsilateral renal anomaly [PDF]

open access: yes, 2018
Herlyn-Werner-Wunderlich Syndrome, otherwise known as obstructed hemivagina and ipsilateral renal anomaly (OHVIRA), is a rare Müllerian anomalyconsisting of uterine didelphys, hemivaginal septum, and ipsilateral renal agenesis.
Grant, Christopher   +3 more
core   +1 more source

Herlyn-Werner-Wunderlich Syndrome with Central Precocious Puberty: A Case Report [PDF]

open access: yesChildhood Kidney Diseases, 2019
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly of the genitourinary tract comprising uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis.
Jeeho Han   +3 more
doaj   +1 more source

Two Cases of Herlyn-Werner-Wunderlich Syndrome with Severe Dysmenorrhea, One Misdiagnosis and One Missed Diagnosis

open access: yesSurgeries, 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 abdominal
Dongsoo Jeon, Hyo Sang Han, Jeong-A Hong
doaj   +1 more source

A rare case of obstructed hemivagina and ipsilateral renal agenesis syndrome presented with haematocolpos and haematometra [PDF]

open access: yes, 2022
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome is a syndrome characterised by obstructed hemivagina, ipsilateral renal agenesis and uterine didelphys.
Kumar, Geetha M.   +2 more
core   +1 more source

Herlyn-Werner-Wunderlich syndrome: A rare cause of abdominal pain and dyspareunia

open access: yesRadiology Case Reports, 2019
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital disease characterized by Mullerian duct anomalies. The characteristic triad of this syndrome includes didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis (hence, also known ...
Ninad Salastekar, MBBS, MPH   +3 more
doaj   +1 more source

MALFORMACIONES MÜLLERIANAS: A PROPÓSITO DEL SÍNDROME DE OHVIRA. REPORTE DE CASOS

open access: yesRevista Médica de la Universidad de Costa Rica, 2023
El síndrome de OHVIRA (Obstructed Hemivagina and Ipsilateral Renal Anomaly) es caracterizado por un útero didelfo, una hemivagina ciega total o parcial y agenesia renal ipsilateral. En este artículo se describen tres casos clínicos de pacientes femeninas
Marcela Medina García   +2 more
doaj   +1 more source

Obstructed Hemivagina and Ipsilateral Renal Anomaly (OHVIRA): Case report [PDF]

open access: yes, 2022
Background: Hemivaginal obstruction syndrome and ipsilateral renal anomalies are known as Herlyn-Werner-Wunderlich syndrome (HWWs) or better known by the acronym OHVIRA (Obstructed Hemivagina and Ipsilasteral Renal Anomaly).
Bobby Indra Utama   +2 more
core   +1 more source

Late presentation, MR imaging features and surgical treatment of Herlyn-Werner-Wunderlich syndrome (classification 2.2); a case report

open access: yesBMC Women's Health, 2018
Background Herlyn-Werner-Wunderlich syndrome is a very rare congenital genitourinary anomaly characterized by uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Case presentation Authors present a case of Herlyn-Werner-Wunderlich syndrome
Hidayatullah Hamidi, Nilab Haidary
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome: a case report [PDF]

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2015
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital disorder of the Müllerian ducts in which there is uterus didelphys, obstructed hemivagina and unilateral renal agenesis.
Pedro Salomao Piccinini, John Doski
doaj   +2 more sources

Herlyn-Werner-Wunderlich Syndrome: A Case Report

open access: yesJournal of Nepal Medical Association, 2023
Herlyn-Werner-Wunderlich syndrome is a rare Mullerian and mesonephric ductal anomaly characterized by a triad of didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis complex.
Priyanka Vaidya   +2 more
doaj   +1 more source

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