Results 51 to 60 of about 1,327 (186)

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: 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

Herlyn-Werner-Wunderlich Syndrome: Pre-and Post-Surgical MRI and US Findings [PDF]

open access: yes, 2015
Herlyn-Werner-Wunderlich syndrome (HWWS) is a rare congenital anomaly of the female urogenital tract that associates Müllerian duct anomalies with mesonephric duct anomalies.
Jogo, R, Lopes Dias, J
core   +1 more source

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

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

Uterine didelphys with obstructed hemivagina and ipsilateral renal anomaly - OHVIRA syndrome: a rare congenital anomaly [PDF]

open access: yes, 2017
OHVIRA or Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterine anomaly with obstructed hemivagina and ipsilateral renal anomaly.
Nagaraju, Rashmi Mysore, Patil, Bhimarao
core   +2 more sources

Diagnosis and surgical management of Herlyn-Werner-Wunderlich syndrome

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Abdominal pain in the adolescent population is rarely attributed to anatomic variance. Minimal consideration placed on this pathology can present a diagnostic dilemma and delay in care if such options are not investigated.
Jennifer A. Munley, Janice A. Taylor
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

Didelphys uterus: an interesting case report of pregnancy in a rare Mullerian anomaly [PDF]

open access: yes, 2022
Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. A didelphys uterus, also known as a double uterus, is one of the least common amongst the MDAs.
Barkase, Akanksha   +5 more
core   +3 more sources

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