Results 21 to 30 of about 2,384 (209)

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

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 with pyohematocolpos: a case report and review of literature [PDF]

open access: yes, 2023
Herlyn-Werner-Wunderlich syndrome (HWWS) is a rare malformation syndrome of the women reproductive tract characterized by uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis. We report here a case of a 20 year-old patient presented
Habek, Dubravko   +3 more
core   +2 more sources

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

Ohvira syndrome with left radial hemimelia: a rare association [PDF]

open access: yes, 2021
Ohvira syndrome is rare complex anomaly consisting of uterus didelphys, unilateral ipsilateral obstructed hemivagina and ipsilateral renal agenesis.
Rao, Rachana B., T., Jayanthy
core   +2 more sources

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

Malformações Müllerianas: revisão da abordagem atual [PDF]

open access: yes, 2009
The aim of this paper was to discuss the embryological aspects of Müllerian duct anomalies and to analyze the current diagnostic methods and therapy. Müllerian anomalies are congenital defects of the female reproductive tract resulting from failure in ...
RIBEIRO, Sérgio Conti   +6 more
core   +2 more sources

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