Uterus didelphys with double vagina diagnosed during third cesarean section: A case report
SAGE Open Medical Case Reports, 2022 Uterus didelphys is a rare uterine anomaly. It is associated with fetal breech presentation, preterm delivery, and cesarean section. Longitudinal vaginal septum may be associated with uterus didelphys, which may cause dyspareunia and labor obstruction ...
Namkha Dorji +2 more
doaj +1 more source
Rare uterine didelphis and cervical pregnancy
Journal of Experimental and Clinical Medicine, 2021 Due to increased vaginal bleeding, a surgical operation was performed on a woman with cervical pregnancy. A diagnosis of uterine didelphis (UD) was made during surgery. The hypogastric arteries on both sides were ligated. After controlling the bleeding, the 3Department of XXX, University of XXX, XXX Training and Research Hospital, City, Country abdomen
KATIRCI, Yunus +3 more
openaire +2 more sources
Uterine didelphys with concomitant renal anomalies in both mother and fetus
Journal of Pediatric Surgery Case Reports, 2016 Uterine didelphys results from impaired fusion of the paired Müllerian ducts. The incidence of uterine anomalies is believed to be 0.5–2.0% of reproductive-age women, with didelphic uterus accounting for approximately 10%. Uterine didelphys is associated
Maren Boehnke +5 more
doaj +1 more source
Uterine Didelphys in a G4P3+0: A Disturbing Phenomenon at Caesarean Section [PDF]
Women’s Health Bulletin, 2023 Introduction: Uterine didelphys is an exceptionally rare Müllerian duct anomaly that, when incidentally discovered, can be profoundly disconcerting for attending clinicians, patients, and their families.
Abdibasid Ali +3 more
doaj +1 more source
Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal [PDF]
, 2008 BACKGROUND: The prevalence of congenital uterine anomalies in women with reproductive failure remains unclear, largely due to methodological bias. The aim of this review is to assess the diagnostic accuracy of different methodologies and estimate the ...
Cocksedge, K.A. +2 more
core +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 ...
Ilyas, Mohd +2 more
core +1 more source
Genetic background influences tumour development in heterozygous Men1 knockout mice [PDF]
, 2020 Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disorder caused by MEN1 germline mutations, is characterised by parathyroid, pancreatic and pituitary tumours. MEN1 mutations also cause familial isolated primary hyperparathyroidism (FIHP)
Christie, Paul T. +11 more
core +2 more sources
Uterus didelphys complicated with endometrial carcinoma
Medicine, 2022 . Rationale:. The incidence of uterine malformations is low (4%–7%). Currently, the National Comprehensive Cancer Network clinical practice guidelines in oncology recommend minimally invasive surgery for early endometrial cancer.
Liang Chen, MD, PhD +4 more
doaj +1 more source
Herlyn-Werner-Wunderlich Syndrome: Pre-and Post-Surgical MRI and US Findings [PDF]
, 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
A Rare Obstetric Outcome in Uterus Didelphys with Obstructed Hemivagina and Ipsilateral Renal Agenesis [PDF]
, 2012 Background: The unique clinical syndrome of uterus didelphys, obstructed hemivagina, and ipsilateral renal anomaly is very rare and can be quite difficult to recognize because of the enormous heterogeneity in its clinical presentation.
Francisco, C +3 more
core +1 more source