Results 61 to 70 of about 108,746 (186)

Type II Robert's Uterus Presenting as Long‐Standing Secondary Subfertility: Diagnosis Confirmed by Combined Laparoscopy and Hysteroscopy in a Bangladeshi Patient

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, Ayesa Perveen, Tahmina Begum, Nishad Tasnim   +3 more
wiley   +1 more source

Robot‐assisted resection of diaphragmatic and hepatorenal recess peritoneal endometriosis: Two cases and a narrative review

International Journal of Gynecology &Obstetrics, Volume 173, Issue 2, Page 614-623, May 2026.
Abstract In this report, we describe two cases of diaphragmatic endometriosis with concurrent hepatorenal recess peritoneal involvement managed using robotic‐assisted laparoscopic surgery with the da Vinci Xi platform. In both patients, diaphragmatic implants and hepatorenal recess peritoneal lesions were excised en bloc, followed by resection of ...
Xiaoming Guan, Qiannan Yang, Daniel Y. Lovell, Chunhua Zhang   +3 more
wiley   +1 more source

A uterus didelphys with breech presentation in a previously scarred uterus; an incidental finding [PDF]

, 2017
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

Two cesarean deliveries after hemi-hysterectomy due to gestational trophoblastic neoplasia

Taiwanese Journal of Obstetrics & Gynecology, 2018
Objective: Although uterine didelphys per se is not associated with an impaired ability to conceive, the association between uterine anomalies and gestational trophoblastic neoplasia (GTN) remains unclear.
Kentaro Kai, Yasushi Kawano, Mitsutake Yano, Mamiko Okamoto, Eiichi Hori, Kaei Nasu, Hisashi Narahara   +6 more
doaj   +1 more source

Unraveling the Genetic Mysteries of Müllerian Anomalies: Research Approaches and Clinical Significance

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, Xin Hou, Xiangyu Wang, Juan Li, Li Li, Xiangyi Ma   +5 more
wiley   +1 more source

Uterine didelphys in Nili Ravi buffalo-A case report [PDF]

, 2017
The basic aim of the study was to document a case study of uterine didelphys, a rare clinical condition in Nili-Ravi buffalos. An approximately 54 months old buffalo with the history of repeat breeding was brought to the Sahala slaughter house Islamabad.
Mubeen, Muhammad, Awan, Furqan, Iqbal, Umair, Ijaz, Muhammad, Nawaz, Mudussar, Ali, Sadaqat   +5 more
core   +1 more source

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, S. Eleonore Köhler, Gabriela Morosan‐Puopolo, Jill P. J. M. Hikspoors, Wouter H. Lamers   +4 more
wiley   +1 more source

Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome: A case report

Journal of Pediatric Surgery Case Reports, 2023
Background: Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) or Herlyn-Werner-Wunderlich syndrome, is a rare Mullerian duct anomaly with uterus didelphys, unilateral obstructed hemivagina, and ipsilateral renal agenesis.
Mohamed Amin Elgohary, Rushikesh Naik, Mohamed Elkafafi, Hussein Hamed, Yaser Ali   +4 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, S. Eleonore Köhler, Gabriela Morosan‐Puopolo, Jill P. J. M. Hikspoors, Wouter H. Lamers   +4 more
wiley   +1 more source

Randomised comparison of uterine artery embolisation (UAE) with surgical treatment in patients with symptomatic uterine fibroids (REST trial): 5-year results [PDF]

, 2011
Objective: To compare the long-term results of uterine artery embolisation (UAE) with surgery for women with symptomatic uterine fibroids. Design Pragmatic, open, multicentre, randomised trial. Setting Twenty-seven participating UK secondary care centres.
MA Lumsden, Wu, O., O Wu, LE Craig, Khaund, A., Lumsden, M.A., Moss, J.G., Cooper, K.G., A Khaund, KG Cooper, JG Moss, Murray, G.D., Craig, L.E., Murray, L., LS Murray, GD Murray   +15 more
core   +1 more source