Results 51 to 60 of about 1,504,083 (159)

Diagnosis and surgical management of Herlyn-Werner-Wunderlich syndrome

Journal 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

Herlyn-Werner-Wunderlich syndrome : a rare genitourinary anomaly in females : a series of four cases [PDF]

, 2018
We present case series of four patients with an important syndrome known as Herlyn-Werner-Wunderlich syndrome. Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal ...
Khan, Insha, Saldanha, Cimona L., Ilyas, Mohd   +2 more
core   +1 more source

Herlyn-Werner-Wunderlich syndrome

, 2016
Clinical History: A 14-year-old girl presented to the emergency department with a history of increasing pelvic pain, without fever, diarrhea or urinary symptoms. She had menarche at the age of 12 and her menstrual cycles were regular. Physical examination and routine labor...
  +5 more sources

Herlyn-Werner-Wunderlich syndrome presenting with dysmenorrhea: a case report

Journal of Medical Case Reports, 2019
Background Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. The most common presentation is abdominal pain, dysmenorrhea, and abdominal mass secondary
Dilruba Sharmen Nishu, Md. Monir Uddin, Khadija Akter, Shameema Akter, Monira Sarmin, Sartaj Begum   +5 more
doaj   +1 more source

Herlyn-Werner-Wunderlich Syndrome: Case Report [PDF]

Turkiye Klinikleri Journal of Gynecology and Obstetrics, 2017
Herlyn-Werner-Wunderlich syndrome (HWWS) is a rare variant of Müllerian duct anomalies. The classic triad of this syndrome: Obstructed hemivagina, didelphys uterus and ipsilateral renal agenesis. It typically presents with severe and progressive dysmenorrhea starting after menarche that was determined secondary to hematocolpos. Although the exact cause
Taşkın, Mine İslimye, Bülbül, Erdoğan, Üreyen, Eda, Adali, Ertan   +3 more
openaire   +3 more sources

Dysmenorrhoea presentation in Herlyn-Werner-Wunderlich syndrome: A case study

Journal of the Pakistan Medical Association
Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemi-vagina, and ipsilateral renal agenesis.
Maryam Noor Malik, Gulshan Ara, Tasneem Akhtar, Humera Naeem   +3 more
doaj   +1 more source

Diagnosis and Treatment in a Tertiary Hospital of a Series of Complex Genital Malformations Corresponding to Double Uterus with Obstructed Hemivagina and Ipsilateral Renal Agenesis

International Journal of Reproductive Medicine, Volume 2018, Issue 1, 2018., 2018
Aim. To evaluate the clinical features, diagnostic routine, treatment, and prognosis of patients with double uterus with obstructed hemivagina and ipsilateral renal agenesis at a University Hospital. Methods. A retrospective study analyzing the medical charts of outpatients with similar complex genital malformations seen at the University Hospital of ...
Júlia Kefalás Troncon, Júlio César Rosa-e-Silva, Rayssa Miranda, Francisco José Candido-dos-Reis, Omero Benedicto Poli-Neto, Antônio Alberto Nogueira, Hind A. Beydoun   +6 more
wiley   +1 more source

Didelphys Uterus: A Case Report and Review of the Literature

Case Reports in Obstetrics and Gynecology, Volume 2015, Issue 1, 2015., 2015
Background. 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 MDAs. This report discusses a case of didelphys uterus that successfully conceived, carried her
Shadi Rezai, Pameela Bisram, Isamarie Lora Alcantara, Ruchi Upadhyay, Carla Lara, Malvina Elmadjian, Erich Cosmi   +6 more
wiley   +1 more source

Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1716-1718, July 2026.
ABSTRACT GCNT2‐related cataracts is a disorder characterized by bilateral congenital cataracts (CC) of various types (with or without the adult i blood phenotype) and is caused by biallelic variants in GCNT2, which has 3 major isoforms, differentiated by alternative splicing of the first exon (known as exon 1A, B, and C).
Audrey O'Neill, Cindy Bayer, Emily McQuillen, Erica D. Smith, Meghan Towne, Dallas Reed   +5 more
wiley   +1 more source

Successful preterm pregnancy in a rare variation of Herlyn-Werner-Wunderlich syndrome: A case report [PDF]

, 2018
Herlyn-Werner-Wunderlich syndrome (HWWS) is an uncommon congenital anomaly of the female urogenital tract, characterised by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. We reported the difficult pregnancy course complicated by
Piccolo E., Salerno, Mg, Francesco Cucinelli, Eleonora Piccolo, Piccione E., CAPPELLO, STEFANIA, Casadei L., Piccolo, E, Stefania Cappello, Salerno M. G., Piccione, E, Cucinelli F., Emilio Piccione, Casadei, L, Luisa Casadei, Maria Giovanna Salerno, Cucinelli, F, Cappello, S   +17 more
core   +1 more source