DUPLEX UTERUS (DIDELPHYS) [PDF]
Journal of the American Medical Association, 1912 The malformations and deformities of the uterus, varying in degree from the almost complete absence of that organ to the very rare cases of its duplication, known as duplex uterus (dihysteria, didelphys), are of intense interest because of their clinical and pathologic aspects.
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Herlyn–Werner–Wunderlich Syndrome: Presentation and Surgical Management Options for Five Cases [PDF]
, 2015 Background: Herlyn?Werner?Wunderlich syndrome is a rare Müllerian-duct anomaly consisting of uterine didelphys, a unilateral obstructed hemivagina, and ipsilateral renal agenesis.
Abuzeid, Mostafa I. +4 more
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HYSTEROSALPINGOGRAPHY: TECHNIQUE AND APPLICATIONS (VIEW) [PDF]
, 2015 Hysterosalpingography (HSG) is the radiographic evaluation of the uterine cavity and fallopian tubes after the administration of a radio-opaque medium through the cervical canal.
Bakun, O.V. +4 more
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Uterus didelphys with obstructed hemivagina with chronic presentation: a case report [PDF]
, 2017 This is a case report of a 24-year patient who had uterus didelphys with obstructed hemivagina. Clinical manifestations of this case were of progressive dysmenorrhea, abdominal pain after menarche, cyclic difficulty in urination and constipation, with ...
Anant, Monika +3 more
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A rare case of uterus didelphys presented as secondary abdominal pregnancy [PDF]
, 2016 Uterus didelphys is a rare type of uterine malformation with poor obstetric outcome. We report a rare case of ruptured uterus didelphys presenting as secondary abdominal pregnancy which was managed by removal of ruptured uterus along with the omentum to ...
Arya, Arun Kumar +5 more
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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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Intrapelvic hibernoma: an incidental finding
Journal of the Belgian Society of Radiology, 2012 Background: A 26-year-old female patient underwent an MRI examination of the pelvis for better evaluation of a suspected uterus didelphys.
B Arys, A Van Landeghem, G Villeirs
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Twin pregnancy in each half of a didelphys uterus with delayed delivery and review of literature
ScienceOpen Research, 2015 Didelphys uterus results from an incomplete fusion of mullerian ducts and corresponds to the class III of mullerian abnormalities of the American Fertility Society.
Ramanah Rajeev +6 more
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A rare case presentation of an anomalous uterus mimicking ovarian tumour [PDF]
, 2017 Mullerian anomalies occur in 1:1000-3000 females. Uterus didelphys and obstructed hemangioma with a septum contribute to 10% anomalies. Young girls present with severe dysmenorrhea, hematometra, hematocolpos and recurrent pregnancy loss.
M., Mohanambal, sheelaa, Wills G.
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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.
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