WNT4 deficiency—a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: A Case Report [PDF]
, 2017 The pathways leading to female sexual determination in mammals are incompletely defined. Loss-of-function mutations in the WNT4 gene appear to cause developmental abnormalities of sexual differentiation in women and mice.
Biason-Lauber, A. +5 more
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Total laparoscopic hysterectomy with uterine didelphys [PDF]
American Journal of Obstetrics and Gynecology, 2022 P.L. Rosenblatt, H.M. French, S.A. Ward
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Obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) syndrome with imperforate anus
Journal of Pediatric Surgery Case Reports, 2016 OHVIRA syndrome (Obstructed hemivagina with ipsilateral renal agenesis) is a rare Mullerian duct anomaly that results in uterine didelphys, obstructed vaginal vault, and unilateral renal agenesis.
Peter Cosgrove +3 more
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Cervical Ectopic Pregnancy in a 23 Year Old with Uterus Didelphys
Clinical Practice and Cases in Emergency Medicine, 2017 Ectopic pregnancy remains an important diagnosis for the emergency physician to recognize, accounting for up to 2% of all pregnancies and associated with significant morbidity and mortality. Ectopic pregnancies can implant in various sites outside of the
Patrick C. Ng, Kristen S. Kann
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Dilemma in diagnosis of pregnancy in didelphys uterus: a original case report [PDF]
Uterine didelphys is a congenital defect of female genital system that arises from abnormal embryological development of mullerian ducts. A 30-year-old female G4P3L3A0 at 9 weeks POG with uneventful previous three normal term delivery presented to gynae ...
Dogra, Kusum +2 more
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Gynecology 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
Uterus Didelphys Bicollis with Uterine Myomatosis
Uterus didelphys bicollis is a congenital malformation of the female genital tract caused by the failure of the Müllerian ducts to fuse during embryonic development. It represents 5% of uterine malformations, with an estimated prevalence of 5.5 to 6.7% in the general population, 8% in women with infertility, and up to 24% in patients with a history of ...
Rodolfo Barcenas Contreras +5 more
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OHVIRA syndrome and its incomplete variant: multimodality imaging insights from two distinct presentations of Müllerian-renal anomalies [PDF]
Mullerian anomalies such as obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome pose diagnostic challenges due to their embryological variability and diverse clinical presentations.
B. S., Pavan, Pavuluri, Viharika
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A rare case of uterus didelphys with full term pregnancy in left horn [PDF]
, 2017 Uterus didelphys, also known as a duplicated uterus, is an embryological abnormality resulting from complete failure of fusion of Mullerian ducts causing full uterine development to erroneously occur bilaterally.
Bendre, Kirti Rajesh +2 more
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Second-trimester uterine rupture in bicornuate uterus: A case report
Case Reports in Women's HealthUterine rupture is a rare but serious complication that predominantly occurs in the third trimester of pregnancy. It is exceptionally uncommon in the second trimester, particularly in the presence of uterine anomalies such as a bicornuate uterus or ...
Mesfin Ayalew Tsegaye +4 more
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