Results 51 to 60 of about 108,746 (186)

Obstructed Hemivagina and Ipsilateral Renal Anomaly Syndrome Rare Obstructive Uterovaginal Anomaly: A Case Report

Journal of Nepal Medical Association, 2020
Obstructed Hemivagina and Ipsilateral Renal Anomaly syndrome is a rare obstructive uterovaginal anomaly involving both mesonephric and paramesonephric ducts. It usually presents after menarche with non-specific symptoms like pelvic pain, dysmenorrhea, or
Tulasa Basnet, Tarun Pradhan, Punita Yadav, Manoj Kumar Sah, Jyotsna Yadav, Yashaswi Rai, Rashmi Thapa   +6 more
doaj   +1 more source

Dicavitary twin pregnancy in patient with bicornuate bicollis uterine anomaly

Clinical Case Reports, 2023
Key Clinical Message Twin pregnancies in uterine didelphys and uterus bicornuate bicollis represent dicavitary twin pregnancies that can be managed using similar principles.
Mihiri Karunaratne, Dora J. Melber, H. Irene Su, Gladys A. Ramos   +3 more
doaj   +1 more source

Pregnancy in uterus didelphys delivered by caesarean delivery: case report [PDF]

, 2017
Uterus didelphys represents a uterine malformation where the uterus is present as paired organ. There is presence of double uterine bodies with two separate cervices and often a double or septate vagina.
Rao, Sneha S., GS, Anitha, P., Chandralekha   +2 more
core   +1 more source

Diagnosis and surgical management of Herlyn-Werner-Wunderlich syndrome

Journal of Pediatric Surgery Case Reports, 2020
Abdominal pain in the adolescent population is rarely attributed to anatomic variance. Minimal consideration placed on this pathology can present a diagnostic dilemma and delay in care if such options are not investigated.
Jennifer A. Munley, Janice A. Taylor
doaj   +1 more source

Recent advances and clinical applications of 3D printing for female reproductive organ regeneration and gynecological disease

Interdisciplinary Medicine, Volume 4, Issue 5, September 2026.
This comprehensive review highlights the transformative role of 3D printing and bioprinting technologies in the regeneration of female reproductive organs and the treatment of gynecological diseases. Unlike previous overviews that focus narrowly on isolated applications, this work provides an integrative analysis of recent clinical and preclinical ...
Chan Hum Park, In‐Sun Hong
wiley   +1 more source

Uterine didelphys: an incidental finding during caesarean section [PDF]

Mullerian duct anomalies are congenital defects of the female reproductive system resulting from abnormal embryological development. Uterine didelphys occurs due to the failure of embryonic fusion of the Mullerian ducts. This results in the presence of a
Amma, Sai L. S. K., Pillai, Reena N. R., Kutty, Sathiamma P.   +2 more
core   +1 more source

Cost-effectiveness of magnetic resonance-guided focused ultrasound surgery for treatment of uterine fibroids [PDF]

, 2007
OBJECTIVE: To estimate the cost-effectiveness of a treatment strategy for symptomatic uterine fibroids, which starts with Magnetic Resonance-guided Focused Ultrasound Surgery (MRgFUS) as compared with current practice comprising uterine artery ...
Cairns, JA, Brewer, C, Zowall, H, Lamping, DL, Regan, L, Gedroyc, WM, Gedroyc, WMW   +6 more
core   +1 more source

Management of congenital female genital tract anomalies related to primary amenorrhea and/or cyclic abdominal pain: A retrospective cohort study

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 9, Page 1810-1822, September 2026.
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, Sofia Tsiapakidou, Eirini Iordanidou, Georgios Kioussis, Anastasia Vatopoulou, Theodoros Theodoridis   +5 more
wiley   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

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, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Asynchronous twin delivery in uterus didelphys with a 12-week interval: case report and literature review

BMC Pregnancy and Childbirth
Background Uterus didelphys, or“double uterus,”is caused by the failure of Müllerian ducts fusion, eventually forming two uterine cavities, and it is one of the rare uterine malformations.Uterus didelphys and twin pregnancies are extremely rare ...
Huijie Liu, Chunxiao Zhou, Yingxin LV, Gaoxia Dong, Hui Qi   +4 more
doaj   +1 more source