Results 61 to 70 of about 1,660 (186)
The Development of the Human Female Reproductive Tract: Part 2—Vagina
ABSTRACT Urogenital epithelium replaces the original paramesonephric (Müllerian) epithelium in the human fetal vagina. We re‐investigated this cell replacement histologically and with three‐dimensional reconstructions. In the lesser pelvis, both Müllerian ducts fuse to form the uterovaginal canal.
Cindy J. M. Hülsman +4 more
wiley +1 more source
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 ...
Garang Dakjur Lueth +5 more
core +1 more source
Abstract Mid‐trimester pregnancy loss (MTL), defined as a pregnancy loss occurring between 14 + 0 and 21 + 6 weeks of gestation, causes significant physical and emotional distress to women and presents clinical challenges to healthcare professionals. It is acknowledged that in low‐resource settings, this guideline might be applicable to births up to 28
Caroline E. Fox +46 more
wiley +1 more source
A uterus didelphys with breech presentation in a previously scarred uterus; an incidental finding
A didelphic uterus results from failed fusion of the paired mullerian ducts characterized by two separated uterine horns, each with an endometrial cavity and uterine cervix.
B., Shilpa H., Shilpa H. B.
core +1 more source
Trisomy 8 mosaicism (T8M) syndrome is a rare aneuploidy condition affecting 1/25,000–50,000 live births. Affected individuals have highly variable phenotypes from very mild dysmorphism to severe structural anomalies caused by chromosomal mosaicism and possibly undetected molecular aberrations. The utilization of chromosome microarray analysis (CMA) and
Zakia Abdelhamed +11 more
wiley +1 more source
Herlyn–Werner–Wunderlich Syndrome Complicated by Endometriosis: Reports of Two Cases
Background Herlyn–Werner–Wunderlich (HWW) syndrome is a rare hereditary disorder characterized by the presence of a didelphic uterus, obstructed hemivagina, and ipsilateral renal agenesis. The etiopathogenesis of this syndrome is not fully understood. It is typically diagnosed around puberty due to the build‐up of menstrual blood. Nevertheless, in some
Niki Talebian +3 more
wiley +1 more source
Pregnancy in uterus didelphys delivered by caesarean section: a case report
The aim of this study is to report a rare case of pregnancy in uterus didelphys. Mullerian duct anomalies are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts.
Devyani Sawai +11 more
core +1 more source
Uterus didelphys associated with good pregnancy outcomes and an ectopc kidney (Case report)
The case of a 32year old para 3+0, 3 alive with 3 years history of recurrent severe lower abdominal pain is presented. The pain was worse during her monthly cycles and relieved during pregnancy.
Kigbu JH, Dakum NK
doaj +1 more source
This report describes a case of a patient diagnosed with a residual Müllerian duct mass on the uterine surface at our hospital. Through analysis of this case and a review of the literature, we are aimed at reducing the risk of misdiagnosis and optimising treatment protocols for uterine cystic masses.
Wenxin Zhong +6 more
wiley +1 more source
Favorable Pregnancy Outcome in a Dicavitary Twin Gestation: A Case Report and Literature Review
Congenital Müllerian anomalies pose unique risks for complications in pregnancy, particularly in the setting of multifetal gestation. Uterine didelphys with dicavitary twin gestation remains a rare entity with fewer than 10 cases reported in the medical literature.
Sara N. Peters +4 more
wiley +1 more source

