Results 21 to 30 of about 1,660 (186)

Pregnancy and Childbirth in Uterus Didelphys: A Report of Three Cases [PDF]

open access: yesMedicina, 2020
Uterus didelphys is a rare form of congenital anomaly of the Müllerian ducts. The clinical significance of this anomaly of the female reproductive tract is associated with various reproductive issues: increased risk of preterm birth before 37 weeks ...
Stanislav Slavchev   +2 more
doaj   +2 more sources

Didelphys Uterus: A Case Report and Review of the Literature [PDF]

open access: yesCase Reports in Obstetrics and Gynecology, 2015
Background. Mullerian duct anomalies (MDAs) are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts.
Shadi Rezai   +5 more
doaj   +2 more sources

Uterus didelphys with unilateral obstructed hemivagina with hematometrocolpos and hematosalpinx with ipsilateral renal agenesis

open access: yesJournal of Human Reproductive Sciences, 2009
Uterus didelphys with blind hemivagina and ipsilateral renal agenesis (Herlyn Werner-Wunderlich Syndrome) is a rare congenital anomaly. It mostly presents with severe dysmenorrhea and a palpable mass due to unilateral hematocolpos.
Gaurav Jindal   +3 more
doaj   +2 more sources

Twin Pregnancy in a Woman with Uterus Didelphys

open access: yesOnline Journal of Health & Allied Sciences, 2011
Uterus didelphys is one of the congenital uterine anomalies due to defective medial fusion of mullerian ducts. This anomaly is known to have poor reproductive outcome and women with this condition often have to be treated for infertility.
Sohini Bhattacharya,   +1 more
doaj   +1 more source

Uterus didelphys with obstructed hemivagina and ipsilateral renal anomaly (OHVIRA syndrome): A case report

open access: yesJournal 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   +2 more sources

Obstructed hemivagina and ipsilateral renal anomaly syndrome with uterus didelphys (OHVIRA)

open access: yesMiddle East Fertility Society Journal, 2013
To report a case of obstructed hemivagina and ipsilateral renal anomaly (OHVIRA syndrome) with uterus didelphys that has been diagnosed successfully with ultrasound and managed with a single stage vaginoplasty.
Mohamed A.F.M. Youssef
exaly   +3 more sources

Fibroids in obstructed hemivagina and ipsilateral renal anomaly-like syndrome: Successful hysterectomy and vaginal septoplasty in a kidney transplant recipient with uterus didelphys, vaginal septum and renal agenesis. [PDF]

open access: yesInt J Gynaecol Obstet
International Journal of Gynecology &Obstetrics, Volume 174, Issue 1, Page 491-493, July 2026.
Cruz MCM   +5 more
europepmc   +2 more sources

Interval Vaginal Delivery of Term Twins From Bilateral Horns of a Uterus Didelphys: Insight Into Labor Initiation and Progression. [PDF]

open access: yesJ Obstet Gynaecol Res
ABSTRACT Uterus didelphys, characterized by two separate uterine cavities and cervices, is associated with increased obstetric complications. Twin pregnancy with one fetus in each horn is exceptionally rare, often managed by cesarean or resulting in preterm birth.
Hiratsuka D   +5 more
europepmc   +2 more sources

Different endometrial receptivity in each hemiuterus of a woman with uterus didelphys and previous failed embryo transfers

open access: yesJournal of Human Reproductive Sciences, 2018
The aim of this report is to describe the clinical case of a 31-year-old patient with uterus didelphys (double uterus) and primary infertility, who had been through several embryo transfers in the context of an in vitro fertilization (IVF) treatment with
Francisco Carranza   +3 more
doaj   +2 more sources

Delayed Diagnosis of Uterus Didelphys Unicolis with Cervical Atresia in a Forty-Three-Year Old Unmarried Woman with Primary Amenorrhea

open access: yesGynecology Obstetrics & Reproductive Medicine, 2006
Müllerian duct fusion deficiency leads to uterus didelphys. We report the first case of a didelphysunicolis uterus with atretic cervix in a 43-y ear-old unmarried woman with a thirty years history of cyclic lower abdominal pain and primary amenhorrea. On
Ahmet Kale   +2 more
doaj   +1 more source

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