A to Z: Ebstein's Anomaly
Ebstein's anomaly is a rare congenital (present at birth) defect in the right side of the heart. The cause is unknown.
More to Know
Someone with Ebstein's anomaly has a malformed (not formed correctly) and improperly positioned tricuspid valve. The tricuspid valve separates the two chambers on the right side of the heart. In a person with Ebstein's anomaly, the valve doesn't close properly, which causes blood to leak back from the lower chamber (ventricle) to the upper chamber (atrium). This disrupts blood flow and makes the heart work inefficiently, which can lead to enlargement of the right atrium, insufficient red blood supply to the body, or heart failure.
Ebstein's anomaly varies in severity from person to person. A newborn showing signs of the condition may be seriously ill and need surgery while someone whose symptoms don't appear until adulthood may not need any treatment.
Signs and symptoms of Ebstein's anomaly include shortness of breath, fatigue, rapid breathing, failure to grow, swelling in the legs, and a bluish skin color around the lips and nails. The condition is often associated with other heart defects, such as atrial septal defect (ASD), pulmonary (valve) stenosis, and abnormal heart rhythms (arrhythmias).
Keep in Mind
The long-term outlook for people with Ebstein's anomaly varies greatly, but with treatment and close monitoring by a cardiologist, most people with the disorder can go on to live healthy and productive lives.
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