Results 51 to 60 of about 277,660 (218)
Malformações Müllerianas: revisão da abordagem atual [PDF]
, 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
An unusual diagnosis of a bicornuate unicollis uterus [PDF]
, 2008 We present a case of an unusual diagnosis of a bicornuate unicollis uterus mimicking a uterus didelphys with blind hemivagina. Few cases of a bicornuate uterus have been reported with the primary symptom of a paracervical pyocolpos.
Foidart, Jean-Michel +2 more
core +1 more source
A Successful Pregnancy in a Hemihysterectomized Patient–A Case Report
Case Reports in Obstetrics and Gynecology, 2022 Introduction. Didelphys uterus, two separate uterine horns or a double uterus with two separate cervices, is one of several congenital uterine anomalies (CUA), accounting for 5% of CUA.
Sofia Jovina Domingues, Luísa Pinto
doaj +1 more source
Gynecologic Oncology Reports, 2021 The purpose of this study was to investigate the clinical application of intensity-modulated radiotherapy combined with intracavitary radiotherapy for locally advanced cervical cancer complicated with uterus didelphys.
Chengzhi Lei +5 more
doaj +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
Pediatrics and Neonatology, 2012 Herlyn-Werner-Wunderlich (HWW) syndrome is a rare variant of Müllerian duct anomalies consisting of uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis.
Tsung-Hsin Wu +6 more
doaj +1 more source
22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report. [PDF]
, 2016 Deletion in the chromosomal region 22q11 results from the abnormal development of the third and fourth pharyngeal pouches during embryonic life and presents an expansive phenotype with more than 180 clinical features described that involve every organ ...
Ben Ali, N. +6 more
core +1 more source
Case Reports in Women's Health, 2019 Uterine malformations are associated with infertility, recurrent miscarriage and preterm birth, to variable degrees. Accurate classification is crucial to management.
Katherine Adams, Lee Minuzzo
doaj +1 more source
Pregnancy with uterine didelphys and history of recurrent pregnancy loss: Case report
Bali Medical Journal, 2023 Link of Video Abstract: https://youtu.be/H7Y7XoPOUAw Background: Uterine didelphys is an embryologic disorder that arises from the failure of Mullerian duct fusion.
D. Pratama, Budi Wicaksono
semanticscholar +1 more source
Uterine Didelphys in a Pregnant Mother
Open Journal of Obstetrics and Gynecology, 2018 Background: Uterine Didelphys is a rare congenital condition and it can affect both mother and fetus. A 24 year-old patient presented to the emergency room with pelvic pain and a pelvic ultrasound confirmed the presence of Uterine Didelphys. She subsequently became pregnant and was first seen at 21 weeks gestation.
Omeed Paknejad +3 more
openaire +2 more sources