If your baby is born with pulmonary atresia, symptoms will be noticeable soon after birth. Your baby's signs and symptoms may include:

• Blue- or gray-toned skin (cyanosis)
• Fast breathing or shortness of breath
• Easily tiring or being fatigued
• Feeding problems

The heart is divided into four hollow chambers, two on the right and two on the left. In performing its basic job — pumping blood throughout the body — the heart uses its left and right sides for different tasks.

The right side of the heart moves blood to the lungs through vessels called pulmonary arteries. In the lungs, blood picks up oxygen then returns to the heart's left side through the pulmonary veins. The left side of the heart then pumps the blood through the aorta and out to the rest of the body to supply your baby's body with oxygen.

Blood moves through your baby's heart in one direction through valves that open and close as the heart beats. The valve that allows blood out of your baby's heart and into the lungs to pick up oxygen is called the pulmonary valve.

In pulmonary atresia, the pulmonary valve doesn't develop properly, preventing it from opening. Blood can't flow from the right ventricle to the lungs.

Before birth, the improperly formed valve isn't life-threatening, because the placenta provides oxygen for your baby instead of the lungs. Blood entering the right side of your baby's heart passes through a hole (foramen ovale) between the top chambers of your baby's heart, so the oxygen-rich blood can be pumped out to the rest of your baby's body through the aorta.

After birth, your baby's lungs must provide oxygen for his or her body. In pulmonary atresia, without a working pulmonary valve, blood must find another route to reach your baby's lungs.

The foramen ovale usually shuts soon after birth, but may stay open in pulmonary atresia. Newborn babies also have a temporary connection (ductus arteriosus) between the aorta and the pulmonary artery.

This passage allows some of the oxygen-poor blood to travel to the lungs where it can pick up oxygen to supply your baby's body. The ductus arteriosus normally closes soon after birth, but can be kept open with medications.

In some cases, there may be a second hole in the tissue that separates the main pumping chambers of your baby's heart, called a ventricular septal defect (VSD).

The VSD allows a pathway for blood to pass through the right ventricle into the left ventricle. Children with pulmonary atresia and a VSD often have additional abnormalities of the lungs and the arteries that bring blood to the lungs.

If there's no VSD, the right ventricle receives little blood flow before birth and often doesn't develop fully. This is a condition called pulmonary atresia with intact ventricular septum (PA/IVS).

In most cases, the exact cause of a congenital heart defect, such as pulmonary atresia, is unknown. However, several factors may increase the risk of a baby being born with a congenital heart defect, including:

• A parent who has a congenital heart defect
• A mother who is obese before getting pregnant
• Smoking before or during pregnancy
• A mother who has poorly controlled diabetes
• Use of some types of medications during pregnancy, such as certain acne drugs and blood pressure medications

Without treatment, pulmonary atresia is nearly always fatal. Even after surgical repairs, you'll need to carefully monitor your child's health for any changes that could signal a problem.

People with structural heart problems, such as pulmonary atresia, are at a higher risk of infectious endocarditis than the general population. Infectious endocarditis is an inflammation of the valves and inner lining of the heart caused by a bacterial infection.

Even after treatment, people born with pulmonary atresia appear to face a higher risk of certain heart problems, such as abnormal heart rhythms (arrhythmias) and heart failure as adults.