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Complete Transposition of the Great Arteries: Patterns of Congenital Heart Disease in Familial Precurrence
Background—Transposition of the great arteries (TGA) is considered to be associated only rarely with genetic syndromes and to have a low risk of precurrence among relatives of affected patients.Expand
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A prospective observational study of associated anomalies in Hirschsprung’s disease
BackgroundAssociated anomalies have been reported in around 20% of Hirschsprung patients but many Authors suggested a measure of underestimation. We therefore implemented a prospective observationalExpand
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Diagnosis, characterization and outcome of congenitally corrected transposition of the great arteries in the fetus: a multicenter series of 30 cases
To describe the anatomy, associated anomalies and outcome of 30 cases of congenitally corrected transposition of the great arteries (ccTGA) detected prenatally.
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Common arterial trunk in the fetus: characteristics, associations, and outcome in a multicentre series of 23 cases
Objective: To assess the accuracy of prenatal diagnosis, the incidence of extracardiac and chromosomal anomalies, and the perinatal outcome in a population of fetuses with common arterial trunkExpand
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Discrete subaortic stenosis: incidence, morphology and surgical impact of associated subaortic anomalies.
BACKGROUND The association between discrete subaortic stenosis and other subaortic anomalies is a well known but rarely reported occurrence. The aim of this study is to define the incidence,Expand
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Severe ductal constriction in the third‐trimester fetus following maternal self‐medication with nimesulide
This was a multicenter series of 10 cases of constriction of the fetal ductus arteriosus occurring after maternal ingestion of one or two oral doses of nimesulide, which led to emergency delivery inExpand
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Familial recurrence of heart defects in subjects with congenitally corrected transposition of the great arteries
Familial recurrence of congenitally corrected transposition of the great arteries (CCTGA) is considered uncommon. Most of the previous familial studies involved a small number of patients andExpand
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Ventricular septal defect in Down syndrome. Anatomic types and associated malformations.
Ventricular septal defect is a common cardiac anomaly in Down syndrome. To detect the prevalence of anatomic types and associated cardiac malformations we analyzed the echocardiographic andExpand
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Prenatal diagnosis and outcome of isolated vascular rings.
The purpose of this study was to describe our experience in the ultrasound visualization and management of prenatally diagnosed isolated vascular rings. From January 2002 to December 2007, a total ofExpand
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Characteristics, associations and outcome of absent pulmonary valve syndrome in the fetus
To assess in a population of 21 fetuses diagnosed with absent pulmonary valve syndrome (APVS) the accuracy of prenatal diagnosis, the incidence of extracardiac and chromosomal anomalies and theExpand
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