Results 11 to 20 of about 1,504,033 (148)

Herlyn–Werner–Wunderlich syndrome

Medical 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, B S Duggal, Nikita Gonnade, Sanjay Khaladkar   +3 more
doaj   +2 more sources

An Unexpected Cause of Pelvic Pain in a Pubertal Case: Herlyn-Werner-Wunderlich Syndrome

Haseki Tıp Bülteni, 2014
Uterovaginal duplication with imperforated hemivagina is a rare type of Mullerian anomaly. If ipsilateral renal agenesis is associated with this complex genital malformation, it is called Herlyn-Werner-Wunderlich syndrome.
Yasemin Kayadibi, Elmar Bayraktarov, Evrim Özmen, Altay Gezer, İbrahim Adaletli   +4 more
doaj   +2 more sources

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

Childhood 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. Case report

Taiwanese Journal of Obstetrics & Gynecology
Objective: Describe a clinical case of a patient with Herlyn Werner Wunderlich Syndrome in whom an accurate diagnosis was not made during menarche due to failures in her care and poor diagnostic suspicion.
Daniel Alberto Reyes-Martinez, Jairo Sneider Galvis-Pabón, Giselly Mayerly Nieves-Cuervo, Edgar Fabián Manrique-Hernández, Alexandra Hurtado-Ortiz, Maricel Licht-Ardila   +5 more
doaj   +2 more sources

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

Вестник 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, I. M. Kagantsov, S. A. Karavaeva, N. A. Kokhreidze   +3 more
doaj   +2 more sources

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

Surgeries, 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

An interesting case of Herlyn–Werner–Wunderlich syndrome

Tzu Chi Medical Journal, 2020
Herlyn–Werner–Wunderlich syndrome (HWWS) is a rare congenital anomaly characterized by uterus didelphys with blind hemivagina and ipsilateral renal agenesis.
Maureen P Tigga
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]

Reproductive Medicine
Background: Mullerian duct anomalies include a broad spectrum of genital tract defects that arise from developmental abnormalities of the genital tract.
Cristina Taliento, Alba Rondoni, Gennaro Scutiero, Matteo Pavone, Matteo Mordenti, Giuseppe Vizzielli, Pantaleo Greco   +6 more
doaj   +5 more sources

Magnetic resonance imaging diagnosis of Herlyn-Werner-Wunderlich syndrome

Medical 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

Proceedings 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, Narasimhan Kannan Laksmi   +1 more
doaj   +2 more sources