Successful preterm delivery in a patient with bicornuate uterus and right renal agenesis: Diagnostic and clinical perspectives [PDF]
Radiology Case ReportsMüllerian duct anomalies can occur during embryogenesis as complex developmental defects of the uterus and other female reproductive organs. This article reports a rare case of bicornuate uterus and right renal agenesis.
Soheil Mirzaei, PhD, Zahra Motaghed, PhD
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Comparison of Different Classification Systems for Müllerian Duct Anomalies: A Retrospective Observational MRI Study [PDF]
MedicinaBackground and Objectives: Müllerian duct anomalies (MDAs) are congenital malformations of the female genital tract for which several classification systems have been proposed.
Laura D’hoore +4 more
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Unclassified Mullerian Anomaly: Retroperitoneal Uterus [PDF]
Women Health Care and Issues, 2021 Anomalies of uterus might be encountered at Caesarean Section or routine investigation. In this article, we present a rare case of double horns of uterus completely separated. One of them is situated retroperitoneally. Therefore, MRI or CT scans is recommend for unclassified Mullerian anomalies, to confirm pelvic or other anomalies and to reduce the ...
Tae-Hee Kim, Jae Hong Sang
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Cervical Dysgenesis: A Rare Mullerian Duct Anomaly [PDF]
Cureus, 2021 Cervical agenesis or dysgenesis is a rare congenital anomaly. The patients usually present with primary amenorrhoea, primary infertility, and cyclical abdominal pain or with a history of prior surgeries like hymenectomy, vaginoplasty, or adhesiolysis for endometriosis along with well developed secondary sexual characters.
Samantaray, Subha R, Mohapatra, Ipsita
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Surgical management of an obstructive Müllerian Anomaly in a patient with anorectal malformation
Journal of Pediatric Surgery Case Reports, 2021 Müllerian duct anomalies are rare in the general population, occurring in less than 3% of women, but much more prevalent in female patients with anorectal malformation, occurring in up to 30% of these patients.
Christina M. Theodorou +4 more
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Successful pregnancy in Didelphys uterus: a case report [PDF]
Majallah-i Zanān, Māmā̓ī va Nāzā̓ī-i Īrān, 2021 Introduction: Didelphys uterus is one of the rare cases of mullerian anomalies that in most cases, remains asymptomatic until pregnancy and delivery. In women with mullerian anomalies, pregnancy and delivery are associated with more complications such as
Laya Shirinzadeh, Maliheh Rakhshanifar
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Case Report: Uterine Anomalies in Girls With a Congenital Solitary Functioning Kidney
Frontiers in Pediatrics, 2021 Unilateral renal agenesis and multicystic dysplastic kidney, resulting in a contralateral solitary functioning kidney (SFK), are part of the broad spectrum of congenital anomalies of the kidney and urinary tract (CAKUT).
Mark J. C. M. van Dam +3 more
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Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence:two case reports and a review of the literature [PDF]
, 2016 Background: The vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association and Mayer-Rokitansky-Küster-Hauser syndrome are rare conditions.
Bjørsum-Meyer, T. +3 more
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MRI IMAGING APPEARANCE IN MULLERIAN DUCT ANOMALIES.
Ain Shams Medical Journal, 2023 Abstract Background Müllerian duct anomalies include a complex spectrum of anatomical anomalies that arise from deviations during the normal development of the Müllerian ducts. In paediatrics, such defects cannot present with any clinical symptoms before puberty, yet, they can also have obstructive ...
Naglaa Hussein Shebreya +2 more
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Ovarian dysgerminoma with Müllerian anomaly: a case report [PDF]
Obstetrics & Gynecology Science, 2020 Müllerian anomalies are rare deformities in women, and only a few cases concerning gynecologic malignancies arising in patients with congenital uterine malformations have been reported. Herein, we present the case of a 34-year-old woman with dysgerminoma
Ha Na Kim +8 more
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