Journal of Human Reproductive Sciences, 2020 Mullerian anomalies which cause infertility in women were described by different classification systems. We report a rare case of uterine anomaly in a 16-year-old patient presented with primary amenorrhea. Her diagnostic laparoscopy findings revealed two
Kamala Selvaraj +2 more
doaj +1 more source
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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A Müllerian cyst in a male adolescent: a case report and literature review
Journal of International Medical Research, 2021 Müllerian duct cyst is a congenital anomaly that originates from an abnormality in the degradation of the Müllerian system and remnants of the Müllerian duct. Müllerian cyst is rarely reported in male adolescents younger than 18 years of age.
Jun He, Kaifa Tang
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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
doaj +1 more source
Müllerian duct anomaly with congenital rectovaginal fistula: A rare case presentation
South African Journal of Obstetrics and Gynaecology, 2015 Pregnancy in a rudimentary horn is a rare form of ectopic gestation and associated with high maternal mortality. Unicornuate uterus with a rudimentary horn is caused by disordered fusion of Müllerian ducts during embryonic life, which can be associated with ipsilateral renal agenesis, congenital rectovaginal fistula, imperforate anus, hypospadias and ...
Yogita Dogra +2 more
openaire +4 more sources
Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal [PDF]
, 2008 BACKGROUND: The prevalence of congenital uterine anomalies in women with reproductive failure remains unclear, largely due to methodological bias. The aim of this review is to assess the diagnostic accuracy of different methodologies and estimate the ...
Cocksedge, K.A. +2 more
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Congenital scoliosis associated with agenesis of the uterine cervix. Case report [PDF]
, 2004 Background: Alterations in the normal sequence of development of müllerian ducts lead to a wide spectrum of reproductive tract abnormalities. A rare form of lack of development, regarding a short tract of the müllerian ducts, leads to the isolated ...
Giorgio Carlomagno +10 more
core +2 more sources
Müllerian duct anomalies with term pregnancy: a case report
Journal of Medical Case Reports, 2020 Background Müllerian duct anomaly is a rare condition. Many cases remain unidentified, especially if asymptomatic. Thus, it is difficult to determine the actual incidence.
Engku Ismail Engku-Husna +2 more
doaj +1 more source
Sex assignment in conditions affecting sex development [PDF]
, 2017 The newborn infant with atypical genitalia presents a challenging clinical scenario and requires expert input. There have been appreciable advances in our knowledge of the underlying causes that may lead to a mere difference or a more serious disorder of
Ahmed, S. Faisal, Markosyan, Renata
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Complete Bicornuate Uterus with Complete Longitudinal Vaginal Septum
Journal of Nepal Medical Association, 2010 Bicornuate Uterus is a type of lateral fusion disorder of the mullerian ducts. According to the American Fertility Society Classification of Mullerian Anomalies, bicornuate uterus is a class IV anomaly. Incidence of this anomaly varies. This may affect a
A Suwal, A Kumar
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