Congenital Heart Anomaly

Congenital Heart Anomaly is a Congenital Heart Defect (CHD) or a congenital heart disease refers to the problem in the structure of heart from birth. Most congenital heart problems do not occur with diseases. Symptoms vary from none to life-threatening depending upon the specific type of problem. There may be different causes for CHD such as infections during pregnancy, parents being closely related, poor nutrition, etc. A number of genetic conditions including Down syndrome, Turner syndrome, Marfan syndrome are also associated with heart defects, Cyanotic heart defects, Non-cyanotic heart defects, Pregnancy infections, Rubella vaccination etc. A coronary artery anomaly (CAA) is a defect in one or more of the coronary arteries of the heart. The defect is congenital (present at birth). CAAs may relate to the origin or the location of the coronary artery. However, the term CAA can be used to describe any defects in a coronary artery, such as an abnormal size or shape. They are often found in patients with other congenital heart diseases  another name for a CAA is an anomalous coronary artery (ACA). A congenital heart defect is a problem with the structure of the heart. It is present at birth. Congenital heart defects are the most common type of birth defect. The defects can involve the walls of the heart, the valves of the heart, and the arteries and veins near the heart. They can disrupt the normal flow of blood through the heart. The blood flow can slow down, go in the wrong direction or to the wrong place, or be blocked completely. Doctors use a physical exam and special heart tests to diagnose congenital heart defects. They often find severe defects during pregnancy or soon after birth.

  • Neonatal lupus syndrome
  • Fetal heart block in pregnancy
  • Congenital heart block with Sjögren syndrome

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Congenital Heart Anomaly Conference Speakers

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