Results 41 to 50 of about 1,660 (186)
Uterine Didelphys in a G4P3+0: A Disturbing Phenomenon at Caesarean Section [PDF]
Women’s Health Bulletin, 2023 Introduction: Uterine didelphys is an exceptionally rare Müllerian duct anomaly that, when incidentally discovered, can be profoundly disconcerting for attending clinicians, patients, and their families.
Abdibasid Ali +3 more
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Uterus didelphys with a successful term pregnancy
, 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
Dhaiya, Soniya, Anand, Smriti
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Philippine Journal of Obstetrics and Gynecology, 2021 Muüllerian duct anomalies (MDAs) are congenital defects arising from probable teratogenic assault at 6–22 weeks of gestation. Uterine didelphys arises from complete lack of fusion of Muüllerian ducts, resulting in two entirely separate hemiuteri ...
Ivy Grace C. Lim +2 more
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Rupture Uterus in Pregnancy with Didelphys Uterus: A Rare Case Report
, 2011 Uterus didelphys is rare and sometimes not even diagnosed. We report a case of didelphys uterus in a 26-year-old pregnant lady who previously had three successful pregnancies with previous one C-section and remained undiagnosed till she presented to us ...
Shaifali Dadhich +2 more
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Membranous dysmenorrhea and decidual casts: A scoping review
International Journal of Gynecology &Obstetrics, EarlyView.Abstract Background Membranous dysmenorrhea, characterized by the expulsion of intact endometrial tissue rather than gradual dissolution during menstruation, occasionally presents as a decidual cast—a complete triangular mold of the uterine cavity. This poorly understood condition is likely underdiagnosed.
Lovisa Brehmer, Hedvig Engberg
wiley +1 more source
Taiwanese Journal of Obstetrics & Gynecology, 2006 Objective: Uterus didelphys with hemivaginal atresia and ipsilateral renal agenesis is a rare syndrome of müllerian anomalies. Term pregnancy at the site of atresia is even rarer.
Fang-Ping Chen, Koon-Kwan Ng
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Acta Obstetricia et Gynecologica Scandinavica, EarlyView.Overall, 21 patients with uterine, cervical, and vaginal aplasia were treated successfully with neovagina formation. In 6 out of 8 patients, with obstructed uterine cavity, anastomosis was successful; one underwent hysterectomy and one elective hemi‐hysterectomy.
Grigoris F. Grimbizis +5 more
wiley +1 more source
American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Robert's uterus is a rare congenital Müllerian duct anomaly characterized by an asymmetric septum dividing the uterine cavity into a communicating and a blind hemicavity despite a normal external contour. Although fewer than 200 cases have been reported globally, the incremental novelty of individual case reports lies in unique clinical ...
Iftekhar Ahmed Sakib +3 more
wiley +1 more source
Uterus didelphys with multiple fibroids: A case report
, 2012 Uterine anomalies are congenital malformations caused by fusion or resorption defects during embryogenesis. Uterus didelphys, or a double uterus, is a rare condition that occurs in female fetuses as they develop in the womb. Here we report a case of a 46
Mohammed Shazly Dr, Sherif Abd El- Karim +11 more
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