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Tetralogy of Fallot (TOF), formerly known as Steno-Fallot tetralogy, [9] is a congenital heart defect characterized by four specific cardiac defects. [4] Classically, the four defects are: [ 4 ] Pulmonary stenosis , which is narrowing of the exit from the right ventricle;
Digital clubbing with cyanotic nail beds in an adult with tetralogy of Fallot. Signs and symptoms are related to type and severity of the heart defect. Symptoms frequently present early in life, but it is possible for some CHDs to go undetected throughout life. [15]
English: What is Tetralogy of Fallot? Tetralogy of Fallot (TOF) is a congenital heart condition characterized by four heart abnormalities—stenosis in the right ventricular outflow tract, right ventricular hypertrophy, ventricular septal defect, and aortic override of septal defect. Together, these can cause cyanosis in the newborn.
Tetralogy of Fallot is actually the most common cause of cyanotic congenital heart defects, accounting for about 50-70%, as well as about 10% of all congenital heart defects in general. Now, it’s not quite clear why some babies develop TOF but it is associated with chromosome 22 deletions and DiGeorge syndrome.
Tetralogy of Fallot: pulmonary stenosis, ventricular septal defect, right ventricular hypertrophy, overriding aorta: Tetralogy of Fallot Ménière's disease: vertigo, tinnitus, fluctuating low frequency hearing loss, aural fullness: Ménière's disease zoonotic tetrad: scrub typhus, chiggers, rodents and birds, scrub vegetation
Severe tricuspid regurgitation with symptoms; Transient ischemic attack or stroke; The CCS further recommends patients who require operation for Ebstein's anomaly should be operated on by congenital heart surgeons who have substantial specific experience and success with this operation. Every effort should be made to preserve the native ...
4 Tetra- prefix: Tetralogy of Fallot; 5 Words: Total anomalous pulmonary venous return; A mainstem intubation with an endotracheal tube can lead to right-to-left shunting. [citation needed] This occurs when the tip of the endotracheal tube is placed beyond the carina. In this way only one lung is oxygenated and oxygen-poor blood from the non ...
The most typical form of APVS is a tetralogy of Fallot variant, [4] however, case studies have linked APVS to several different congenital cardiac syndromes, such as agenesis of ductus arteriosus, [5] persistent ductus arteriosus, [6] atrioventricular septal defect, [7] pulmonary branching abnormalities, [8] [9] transposition of the great arteries, [10] and type B interrupted aortic arch. [11]