tetralogy of Fallot


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tetralogy of Fal·lot

 (fă-lō′)
n.
A congenital malformation of the heart characterized by a defect in the ventricular septum, misplacement of the origin of the aorta, narrowing of the pulmonary artery, and enlargement of the right ventricle.

[After Étienne Fallot (1850-1911), French physician.]
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.tetralogy of Fallot - a congenital heart defect producing cyanosis; characterized by four symptoms: pulmonary stenosis and ventricular septal defect and malposition of the aorta over both ventricles and hypertrophy of the right ventricle
pulmonary stenosis - abnormal narrowing of the opening into the pulmonary artery from the right ventricle
syndrome - a pattern of symptoms indicative of some disease
congenital heart defect - a birth defect involving the heart
ventricular septal defect - a common congenital heart defect; an abnormal opening in the septum dividing the ventricles allows blood to pass directly from the left to the right ventricle; large openings may cause congestive heart failure
Translations

tetralogy of Fallot

n tetralogía de Fallot
References in periodicals archive ?
The surgeon mentioned that all babies with Tetralogy of Fallot
Cardiac MR Imaging Assessment Following Tetralogy of Fallot Repair.
The surgeon mentioned that all babies with Tetralogy of Fallot need corrective surgery as without treatment, the child might not grow and develop properly.
All babies who have Tetralogy of Fallot need corrective surgery.
Key Words: Tetralogy of Fallot, Pulmonary artery variants.
HIRA gene is lower expressed in the myocardium of patients with tetralogy of Fallot.
Methods: In this retrospective study, 307 cases of primary repair of Tetralogy of Fallot were done between September 2012 to February 2017, at CPE Institute of cardiology, Multan.
The ratio of cardiac problems is 30% among patients with TAR syndrome, and the most common heart defects are tetralogy of Fallot (17.
Cardiovascular malformations were diagnostically categorized in the following nine subtypes: ventricular septal defect, atrial septal defect, patent ductus arteriosus, coarctation of aorta, pulmonary valve stenosis, tetralogy of Fallot, hypoplastic left heart syndrome, transposition of conducting arteries, and other uncommon subtypes such as ectopia cordis, ventricular double outlets, tricuspid atresia, inborn aortic arch anomalies, and others.
Conclusion: Transcatheter coil occlusion of MAPCAs is effective and hameodynamically beneficial interventional therapy in patients of total correction for Tetralogy of Fallot.
At just 10 months old, Elki was diagnosed with Tetralogy of Fallot - a form of congenital heart disease, which sees four structural abnormalities occur within the heart.
Additionally, she was found to have tetralogy of Fallot.