Results 41 to 50 of about 1,504,033 (148)

Herlyn-Werner-Wunderlich syndrome: a case report

, 2022
Herlyn-Werner-Wunderlich Syndrome is a congenital anomaly of mullerian ducts, characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis which can lead to progressive dysmenorrhea in post menarche, hematocolpos or ...
Ahmetgjekaj, Ilir, Kutllovci, Arben, Bajraktari, Edita   +2 more
core   +1 more source

A Case Report of Herlyn-Werner-Wunderlich Syndrome [PDF]

, 2023
Introduction Müllerian duct abnormalities (MDAs) are the most common congenital genital abnormalities in females and included defects ranging from minor anomalies such as bicornuate or septate uterus to major defects such as uterus aplasia (1)Herlyn ...
Hosseini, Afsaneh
core   +1 more source

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 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: a case report [PDF]

Revista 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   +2 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