Results 21 to 30 of about 2,413 (204)

Case report: Double uterus in young women delivered by Caesarean Section: five cases from South Sudan and Ethiopia

open access: yesSouth Sudan Medical Journal, 2022
Double uterus (uterus didelphys) is the second least common congenital anomaly of the female genital tract resulting from failure of fusion of the two Müllerian ducts during embryological development, leading to duplication of the uterus and the cervix ...
Jok Thikuiy Gang   +2 more
doaj   +1 more source

Ovarian dysgerminoma with Müllerian anomaly: a case report [PDF]

open access: yesObstetrics & Gynecology Science, 2020
Müllerian anomalies are rare deformities in women, and only a few cases concerning gynecologic malignancies arising in patients with congenital uterine malformations have been reported. Herein, we present the case of a 34-year-old woman with dysgerminoma
Ha Na Kim   +8 more
doaj   +1 more source

Uterus didelphys associated with ovarian endometriosis in an infertile patient [PDF]

open access: yesVojnosanitetski Pregled, 2019
Introduction. Uterus didelphys results when Mullerian duct fusion is completely arrested during development. We presented a rare case of nonobstructive uterus didelphys occurring simultaneously with an endometriotic cyst of the ovary. Case report.
Rudić-Biljić-Erski Ivana   +4 more
doaj   +1 more source

Successful pregnancy in Didelphys uterus: a case report [PDF]

open access: yesMajallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, 2021
Introduction: Didelphys uterus is one of the rare cases of mullerian anomalies that in most cases, remains asymptomatic until pregnancy and delivery. In women with mullerian anomalies, pregnancy and delivery are associated with more complications such as
Laya Shirinzadeh, Maliheh Rakhshanifar
doaj   +1 more source

Didelphys Uterus in Pregnancy, an Uncommon Mullerian Duct Anomaly: A Case Report

open access: yesClinical Practice and Cases in Emergency Medicine, 2021
Introduction: Didelphys uterus, or “double uterus,” is one of the rarest Müllerian duct anomalies (MDA). Due to its rarity, data are sparse on overall outcomes associated with this congenital defect, but it may be associated with several complications ...
Colin Jorgensen, Monika Lusiak
doaj   +1 more source

Laparoscopic excision and repair of a cesarean scar pregnancy in a woman with uterine didelphys: a case report [PDF]

open access: yesJournal of Yeungnam Medical Science, 2023
Cesarean scar pregnancy (CSP) is a rare complication that occurs in less than 1% of ectopic pregnancies, and uterine didelphys is one of the rarest uterine forms.
Seong-Eon Park, Ji-Eun Ryu, Tae-Kyu Jang
doaj   +1 more source

Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal [PDF]

open access: yes, 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]

open access: yes, 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

Herlyn-Werner-Wunderlich Syndrome: Pre-and Post-Surgical MRI and US Findings [PDF]

open access: yes, 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]

open access: yes, 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

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