Results 71 to 80 of about 1,660 (186)

Case Report: Effective Pregnancy Management in Uterus Didelphys [PDF]

open access: yes
Introduction: Uterus didelphys is a rare congenital anomaly resulting from incomplete fusion of the Müllerian ducts, accounting for 10% of such anomalies. It often goes unnoticed until reproductive age, sometimes causing dyspareunia or dysmenorrhea. This
Lubis, Munawar Adhar, Fakhrizal, Edy
core   +1 more source

Didelphys uterus: an interesting case report of pregnancy in a rare Mullerian anomaly

open access: yes, 2022
Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts. A didelphys uterus, also known as a double uterus, is one of the least common amongst the MDAs.
Niranjan N. Chavan   +11 more
core   +1 more source

Intestinal Atresia in PPP1R12A ‐Related Urogenital and Brain Malformation Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT PPP1R12A‐related urogenital and brain malformation syndrome (UBMS) is a newly described disorder characterized by congenital anomalies primarily involving the urogenital system and the brain. We describe a preterm female neonate with multiple congenital anomalies, including type IIIb jejunal atresia, incomplete intestinal rotation, imperforate
Adriana Gomes   +4 more
wiley   +1 more source

Late presentation, MR imaging features and surgical treatment of Herlyn-Werner-Wunderlich syndrome (classification 2.2); a case report

open access: yesBMC Women's Health, 2018
Background Herlyn-Werner-Wunderlich syndrome is a very rare congenital genitourinary anomaly characterized by uterus didelphys, blind hemivagina and ipsilateral renal agenesis. Case presentation Authors present a case of Herlyn-Werner-Wunderlich syndrome
Hidayatullah Hamidi, Nilab Haidary
doaj   +1 more source

Spontaneous pregnancy at term with uterus didelphys: a case report

open access: yes, 2018
The uterus didelphys results from the absence of fusion of the bilateral mullerian ducts. It is a rare pathology. This malformation concerns 5% of uterine malformations from mullerian ducts and affects one woman in 1,000-30,000. Obstetrical complications
IA, Housni   +6 more
core   +1 more source

FIGO good practice recommendations on preconception care: A strategy to prevent preterm birth

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 171, Issue 2, Page 574-587, November 2025.
Abstract Preterm birth (PTB) remains one of the leading causes of neonatal mortality and long‐term morbidity worldwide, with minimal progress being made in reducing its incidence, particularly in low‐resource settings. Preconception care is recognized as an effective strategy for PTB prevention; however, the fact that more than half of pregnancies ...
Leticia Irma Ojeda   +21 more
wiley   +1 more source

Uterus didelphys with pregnancy and its different maternal and perinatal outcomes

open access: yes, 2017
Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts.
Soni Mourya   +5 more
core   +1 more source

Uterus didelphys bicollis bicolpos —A case report

open access: yes
Uterus didelphys refers to a congenital uterine anomaly that occurs due to failed fusion of the paired Müllerian ducts. It is characterized by two separate noncommunicating uterine horns each with its cervix and fallopian tube. Duplication may be limited
Oindi, Felix, Nyagaka, Felix
core   +1 more source

Intrapelvic hibernoma: an incidental finding

open access: yesJournal of the Belgian Society of Radiology, 2012
Background: A 26-year-old female patient underwent an MRI examination of the pelvis for better evaluation of a suspected uterus didelphys.
B Arys, A Van Landeghem, G Villeirs
doaj   +1 more source

Twin pregnancy in each half of a didelphys uterus with delayed delivery and review of literature

open access: yesScienceOpen Research, 2015
Didelphys uterus results from an incomplete fusion of mullerian ducts and corresponds to the class III of mullerian abnormalities of the American Fertility Society.
Ramanah Rajeev   +6 more
doaj   +1 more source

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