Results 21 to 30 of about 369,616 (163)
Distal-less homeobox genes Dlx5/6 regulate Müllerian duct regression
, 2022 Dlx5 and Dlx6 encode distal-less homeodomain transcription factors that are present in the genome as a linked pair at a single locus. Dlx5 and Dlx6 have redundant roles in craniofacial, skeletal, and uterine development.
Behringer, Richard R +7 more
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Magnetic resonance imaging in diagnosis and classification of uterovaginal congenital anomalies
Medical Journal of Dr. D.Y. Patil University, 2017 Uterine congenital anomalies are clinically relevant because these are associated with increased incidences of infertility and menstrual disorder. These are frequently not diagnosed at birth.
Pratiksha Yadav
doaj +1 more source
Journal of Medical Case Reports, 2021 Background Müllerian duct anomalies are congenital malformations of the female genital tract and may be of various types. For decades they have been classified according to the American Society of Reproductive Medicine, which mentions unicornuate uterine
G. Gitas +6 more
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The Egyptian Journal of Radiology and Nuclear Medicine, 2021 Background Maldescended ovaries are a rare condition. Despite its different embryologic development with the uterus, maldescended ovary is usually accompanied by uterine malformations and is found during the course of infertility.
Nima Rakhshankhah +4 more
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Lhx1 is required in Müllerian duct epithelium for uterine development [PDF]
, 2014 The female reproductive tract organs of mammals, including the oviducts, uterus, cervix and upper vagina, are derived from the Müllerian ducts, a pair of epithelial tubes that form within the mesonephroi.
Kwan, Kin Ming +3 more
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The Herlyn-Werner-Wunderlich Syndrome: a Rare Case Report [PDF]
Journal of Liaquat National Hospital, 2023 Obstructed Hemivagina and Ipsilateral Renal Agenesis (OHVIRA) is an aberrated and special type of Mesonephric duct malformation and Müllerian duct anomaly. This mostly reports 5% of Müllerian duct anomalies. The majority of cases of OHVIRA are presented
Uzma Panhwer +4 more
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Cellular mechanisms of Müllerian duct formation in the mouse [PDF]
, 2007 Regardless of their sex chromosome karyotype, amniotes develop two pairs of genital ducts, the Wolffian and Müllerian ducts. As the Müllerian duct forms, its growing tip is intimately associated with the Wolffian duct as it elongates to the urogenital ...
Richard R. Behringer +3 more
core +1 more source
Successful Pregnancy Outcome in Uterus Didelphys: A Rare Case Report
Journal of College of Medical Sciences-Nepal, 2023 Didelphys uterus is a mullerian duct anomaly that is extremely rare and has unpredictable reproductive and gestational effects. Common genital tract congenital defects in women can have a wide range of implications.
Sharmila Poudel
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Successful Pregnancy Outcome after Open Strassman Metroplasty for Bicornuate Uterus
Case Reports in Obstetrics and Gynecology, 2018 Introduction. Müllerian duct anomalies represent a group of congenital malformations that result from failure to complete bilateral paramesonephric duct elongation, fusion, canalization, or septal resorption.
Edgar Gulavi +3 more
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Twin gestation in a uterus didelphys with only one functional cervix: A case report
Case Reports in Women's Health, 2019 Introduction: Twin gestation in a uterus didelphys with one fetus in each uterine cavity is rare and presents unique challenges in antepartum and intrapartum care. Case Presentation: A 35-year-old woman with a uterus didelphys became pregnant with twins,
Rebecca J. Post +2 more
doaj +1 more source