Results 31 to 40 of about 960 (145)

Abdominopelvic Pain in Patient with Uterus Didelphys and Unilateral Obstructed Hemivagina and Ipsilateral Renal Agenesis (OHVIRA Syndrome) [PDF]

open access: yes, 2021
Introduction: Uterus didelphys with obstructed hemivagina associated with ipsilateral renal agenesis (OHVIRA syndrome) is a rare female urogenital malformation and delay in its diagnosis could lead to several complications. Case presentation: A 21 ...
Montazeri, Ali, Tavoli, Zahra
core   +2 more sources

Herlyn-Werner-Wunderlich syndrome: Case report

open access: yesRevista de la Facultad de Medicina, 2021
Introduction: Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation of the urogenital tract characterized by the triad of uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis, which is usually diagnosed after ...
Laura Catalina López-Alza   +1 more
doaj   +1 more source

Wunderlich--Herlyn--Werner syndrome [PDF]

open access: yes, 2016
A 25 year old married and nulliparous woman with regular menstrual cycles presented with dyspareunia, infertility, increasing dysmenorrhea and recent onset vulval swelling in the gynaec outpatient department at Bhaskar medical college & Bhaskar ...
Biswas, Sathyakumar   +4 more
core   +2 more sources

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.
Devi, Auxeelia Packia   +2 more
core   +2 more sources

A rare urogenital malformation “Herlyn-Werner-Wunderlich syndrome” (Ohvira syndrome) discovered during an acute pelvic pain [PDF]

open access: yes, 2023
The Herlyn-Werner-Wunderlich syndrome (OHVIRA syndrome) is a rare urogenital malformation, characterized by a blind hemivagina, a didelphic uterus, and homolateral renal agenesis, it results from a defect in the development of the muller and Wolf ducts ...
Ahmed, Mimouni Ahmed   +5 more
core   +2 more sources

The Herlyn-Werner-Wunderlich (HWW) syndrome – A case report with radiological review

open access: yesRadiology Case Reports, 2022
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly of female urogenital tract involving combined mullerian duct anomalies and mesonephric duct malformation characterized by uterus didelphys, obstructed hemi-vagina and ipsilateral renal ...
Abdul Malik Hayat, MD, MPH   +3 more
doaj   +1 more source

An unusual appearance of the post-pubertal Herlyn-Werner-Wunderlich syndrome with acute abdominal pain: A case report [PDF]

open access: yes, 2019
Background: Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital urogenital defect. It is detected by unilateral low vaginal obstruction, uterus didelphys, and ipsilateral kidney agenesis.
Esmailzadeh, Arezoo, Ghasemi, Marzieh
core   +3 more sources

Herlyn–Werner–Wunderlich syndrome

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Herlyn–Werner–Wunderlich syndrome is a rare developmental anomaly, in which there is uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis.
Himadri Bal   +3 more
doaj   +1 more source

management and outcome of herlyn werner wunderlich syndrome conservative treatment in pediatric age [PDF]

open access: yes, 2014
Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital mullerian anomaly consisting of uterus didelphys, hemivaginal septum, and unilateral renal agenesis. Reported data in pediatric age are rare.
A.L. Bulotta   +6 more
core   +1 more source

A Rare Obstetric Outcome in Uterus Didelphys with Obstructed Hemivagina and Ipsilateral Renal Agenesis [PDF]

open access: yes, 2012
Background: The unique clinical syndrome of uterus didelphys, obstructed hemivagina, and ipsilateral renal anomaly is very rare and can be quite difficult to recognize because of the enormous heterogeneity in its clinical presentation.
Francisco, C   +3 more
core   +1 more source

Home - About - Disclaimer - Privacy