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Tricuspid atresia

Tricuspid atresia

Heart, section through the middle
Heart, section through the middle

Definition:

Tricuspid atresia is a type of congenital heart disease in which the tricuspid heart valve is missing or abnormally developed. The defect blocks blood flow from the right atrium to the right ventricle.

Alternative Names:
Tri atresia
Causes, incidence, and risk factors:

Tricuspid atresia is an uncommon form of congenital heart disease that affects about 5 in every 100,000 live births. Twenty percent of patients with this condition will have also have other heart problems.

Normally, blood flows into the right atrium, then through the tricuspid valve to the right ventricle and on to the lungs. If the tricuspid valve is missing or broken, the blood cannot flow from the right atrium to the left ventricle. Blood ultimately cannot enter the lungs, where it must go to pick up oxygen (become oxygenated).

Infants with tricuspid atresia generally are cyanotic (bluish discoloration of skin) and easily become short of breath.

Symptoms:
Signs and tests:

This condition may be discovered during routine prenatal ultrasound imaging or when the baby is examined shortly after birth. Cyanosis may be present from birth. A heart murmur is generally present at birth and may increase in loudness over several months.

Tests may include the following:


Review Date: 12/10/2007
Reviewed By: David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.; and Mark A Fogel, MD, FACC, FAAP, Associate Professor of Pediatrics and Radiology, Director of Cardiac MR, The Children's Hospital of Philadelphia.

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 2002 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

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