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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Embryological basis of malformed female genital tract and various classifications
National Journal of Clinical Anatomy, 2014 Developmental anomalies of the Mullerian duct system represent some of the most fascinating disorders that obstetricians and gynaecologists encounter.
Richa Niranjan, A K Singh, Anjoo Yadav
doaj +1 more source
The Professional Medical Journal, 2012 Background: Müllerian duct anomalies (MDAs) occur with an incidence estimated to be 4.3%. A unicornuate uterus with orwithout a rudimentary horn; is a type of mullerian duct abnormality with a frequency of 0.4%. Rudimentary horn pregnancies are rare obstetriccomplication and may cause difficulty in diagnosis and subsequent management.
SARWAT ARA, TASNEEM ALI
openaire +2 more sources
Journal of Human Reproductive Sciences, 2012 Mullerian duct anomalies, though rare, can be a treatable cause of pelvic pain and infertility. Various complex Mullerian duct anomalies may exist with combination of features of more than one class.
Sanyal Kumar +2 more
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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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Apollo Medicine, 2019 Müllerian duct aplasia–renal agenesis–cervicothoracic somite dysplasia (MURCS) association is a rare and unusual constellation of nonrandom findings that include Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia. The agenesis of
Reddy Ravikanth, Pooja Majumdar
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Herlyn-Werner-Wunderlich syndrome : a rare genitourinary anomaly in females : a series of four cases [PDF]
, 2018 We present case series of four patients with an important syndrome known as Herlyn-Werner-Wunderlich syndrome. Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal ...
Ilyas, Mohd +2 more
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MR assessment of Müllerian duct anomalies: Does it help?
The Egyptian Journal of Radiology and Nuclear Medicine, 2014 Purpose: To evaluate the role of magnetic resonance imaging in diagnosis of Müllerian duct anomalies. Patients and methods: A prospective study included 48 female patients suspected to have Müllerian duct anomalies. All patients underwent trans-abdominal
Nadia F. El Ameen +2 more
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Role of imaging in the diagnosis and management of complete androgen insensitivity syndrome in adults [PDF]
, 2013 Complete androgen insensitivity syndrome is an X-linked recessive androgen receptor disorder characterized by a female phenotype with an XY karyotype.
De Visschere, Pieter +4 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
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