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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;
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 ...
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.
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]
Trilogy of Fallot is a combination of three congenital heart defects: pulmonary stenosis, right ventricular hypertrophy, and an atrial septal defect. [ 1 ] The first two of these are also found in the more common tetralogy of Fallot .
Tetralogy of Fallot; Gastrointestinal and hepatobiliary: Malabsorption; Crohn's disease and ulcerative colitis; Cirrhosis, especially in primary biliary cholangitis [9] Hepatopulmonary syndrome, a complication of cirrhosis [10] Others: Graves' disease (autoimmune hyperthyroidism) – in this case it is known as thyroid acropachy [11]
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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.