Results 51 to 60 of about 2,384 (209)
Placenta Increta With Uterus Didelphys Gravidity: Single Hospital Case Report [PDF]
, 2022 24 years old primigravida has started antenatal care in the TSMU First University Clinic with previously diagnosed uterus didelphys. Normally progressive pregnancy in a right uterus has been confirmed with gestation age 9 week.
Ezieshvili, L +4 more
core +2 more sources
Case Report: History-Indicated McDonald's Cerclage for Uterine Didelphys and History of Cervical Insufficiency. [PDF]
Case Rep Obstet GynecolIntroduction Mullerian anomalies alone are not an indication for prophylactic and history indicated cerclage (HIC). Data on the use of cerclage for patients with mullerian anomalies is therefore limited to case reports of ultrasound indicated cerclage (UIC) and physical exam indicated cerclage (PIC).
Rominger E, Lesser HT, Boozarjomehri F.
europepmc +2 more sources
Clinical Genetics, Volume 109, Issue 4, Page 615-629, April 2026.This review primarily summarizes the genetic defects in Müllerian anomalies, the tools used to validate these genetic defects, and the future clinical significance of identifying the precise genetic etiology of Müllerian anomalies. ABSTRACT Müllerian anomalies are a collection of heterogeneous anatomical disorders of the female genital tract that ...
Jingfang Li +5 more
wiley +1 more source
Uterus didelphys with a successful term pregnancy [PDF]
, 2019 Mullerian duct anomalies are congenital defects of female genital system that arise from abnormal embryological development of mullerianducts. Uterusdidelphys also known as double uterus is one of the least mulleriananomalies. Here we present a case of a
Anand, Smriti, Dhaiya, Soniya
core +2 more sources
The Development of the Human Female Reproductive Tract. Part 1: Uterine Tube and Uterus
Clinical Anatomy, Volume 39, Issue 1, Page 92-111, January 2026.ABSTRACT The uterine tubes and uterus develop from the paramesonephric (Müllerian) ducts. Most experimental data are obtained in rodents. Since the (micro‐)anatomy of the murine urogenital tract differs from that in humans, evaluation of the translatability of mouse data to human development is relevant.
Cindy J. M. Hülsman +4 more
wiley +1 more source
Journal of Pediatric Surgery Case Reports, 2014 Uterus didelphys with obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome is a rare congenital urogenital anomaly. We report a case of a 14-year-old female who presented with acute lower abdominal pain and tender pelvic mass.
Mohamed Amin El-Gohary
doaj +1 more source
Uterine didelphys with dicavitary twin gestation: A case report
Case Reports in Women's Health, 2020 Uterine didelphys is a rare type of congenital uterine anomaly resulting from incomplete fusion of the paramesonephric ducts during embryogenesis. We report the case of a 27-year-old multiparous woman who presented with ovulation-induced dicavitary ...
Alison Laura King +2 more
doaj +1 more source
The Development of the Human Female Reproductive Tract: Part 2—Vagina
Clinical Anatomy, Volume 39, Issue 1, Page 112-131, January 2026.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
A rare case of Herlyn-Werner-Wunderlich syndrome-with pregnancy
The Egyptian Journal of Radiology and Nuclear Medicine, 2016 Herlyn-Werner-Wunderlich syndrome also known as uterus didelphys with obstructing hemivaginal septum and ipsilateral renal agenesis (OHVIRA) is a very rare syndrome with only a few case reported.
Vikas Deswal +3 more
doaj +1 more source
MR ile saptanan uterus didelphys bicollis olgusu
Genel Tıp Dergisi, 2019 Uterus'un nadir görülen varyasyonlarından olan uterus didelphys, müllerian füzyonun gerçekleşmemesi sonucu oluşmaktadır. İlk olarak 1925 yılında Wilson tarafından rapor edilmiştir.
Zeliha Fazlıoğulları +3 more
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