Introduction
Tetralogy of Fallot is a rare but serious heart condition that affects babies at birth. It is one of the most common types of congenital heart disease, which means the baby is born with it. This condition is made up of four heart problems that affect how blood flows through the heart and to the rest of the body.
The four problems in Tetralogy of Fallot are:
Ventricular Septal Defect (VSD): A hole between the two lower chambers of the heart.
Pulmonary Stenosis: Narrowing of the valve that carries blood from the heart to the lungs.
Right Ventricular Hypertrophy: Thickening of the heart muscle on the right side.
Overriding Aorta: The main artery (aorta) sits over the hole in the heart, instead of being connected only to the left side.
These problems reduce the amount of oxygen-rich blood that flows from the heart to the body. As a result, children with Tetralogy of Fallot symptoms may appear blue (called cyanosis) because their blood doesn't carry enough oxygen.
Tetralogy of Fallot causes
The exact cause of Tetralogy of Fallot is not always known, but it can happen if:
1. The baby has a genetic condition like Down syndrome or DiGeorge syndrome.
2. The mother had rubella (German measles) during pregnancy.
3. There is a family history of congenital heart defects.
4. The mother has diabetes or uses certain medications or alcohol during pregnancy.
Tetralogy of Fallot symptoms
Common signs and symptoms include:
1. Bluish skin, lips, and nails (especially during crying or feeding)
2. Trouble breathing or shortness of breath
3. Poor weight gain
4. Fainting or seizures in severe cases
5. Tiring easily during feeding or playing
6. A heart murmur (unusual heart sound)
Early diagnosis and Tetralogy of Fallot treatment are important to prevent serious complications. Most children with this condition will need Tetralogy of Fallot surgery to fix the heart defects.