Results 21 to 30 of about 1,504,083 (159)

Herlyn-Werner-Wunderlich Syndrome: A Mini-review [PDF]

open access: yesChildhood Kidney Diseases, 2018
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation syndrome that is characterized by a triad of uterine didelphys, blind hemivagina, and ipsilateral renal agenesis.
Jiwon M. Lee
doaj   +3 more sources

Herlyn-Werner-Wunderlich Syndrome: Comparison of Two Cases. [PDF]

open access: yesInt J Environ Res Public Health, 2020
Background: Herlyn-Werner-Wunderlich Syndrome is a rare malformation syndrome characterized by uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis. Symptoms appear most often after menarche and are secondary to hematocolpos.
Kozłowski M   +4 more
europepmc   +5 more sources

Urological anomalies in OHVIRA syndrome (Herlyn-Werner-Wunderlich syndrome) [PDF]

open access: yesВестник урологии, 2022
We provide a systematic review of articles related to OHVIRA syndrome (Herlyn-Werner-Wunderlich syndrome), found in PubMed/MedLine, Web of Science, Scopus, Scirus, The Cochrane Library and eLIBRARy to show how the urological component of this congenital ...
K. Lodeikina   +3 more
doaj   +2 more sources

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   +2 more sources

Uterus Didelphys with Hematocervix in the Unilateral Obstructed Hemivagina and Ipsilateral Renal Agenesis: A Case Report of Herlyn–Werner–Wunderlich Syndrome [PDF]

open access: yesReproductive Medicine
Background: Mullerian duct anomalies include a broad spectrum of genital tract defects that arise from developmental abnormalities of the genital tract.
Cristina Taliento   +6 more
doaj   +5 more sources

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   +6 more sources

Magnetic resonance imaging diagnosis of Herlyn-Werner-Wunderlich syndrome

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Herlyn-Werner-Wunderlich syndrome (HWW) is a triad of didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis. It is a combined anomaly of Mullerian and mesonephric ducts.
Taruna Yadav, Padam Parmar
doaj   +2 more sources

Herlyn–Werner–Wunderlich Syndrome: Case report of a newborn presenting with interlabial cyst

open access: yesProceedings of Singapore Healthcare, 2019
A newborn with Herlyn–Werner–Wunderlich Syndrome presented with interlabial cyst. The cyst was punctured and instilled with contrast medium for cystography to demonstrate the anatomy. Simple resection of the hemivagina septum at the same sitting resolved
Yee Ling Cheong   +1 more
doaj   +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   +2 more sources

Herlyn-Werner-Wunderlich syndrome presenting with infertility: Role of MRI in diagnosis

open access: yesIndian Journal of Radiology and Imaging, 2013
Herlyn-Werner-Wunderlich syndrome (HWWS), characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis, is an uncommon combined Mullerian and mesonephric duct anomaly, and its presentation in adulthood is even rarer. We report
Zohra Ahmad   +4 more
doaj   +2 more sources

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