Related Conditions and Treatments
22q11.2 Deletion Syndrome (DiGeorge Syndrome)
Condition
22q11.2 deletion syndrome is a genetic condition that causes a combination of medical problems. These problems may include heart defects, cleft palate, speech or feeding problems, difficulty fighting infections, low calcium levels, kidney problems, learning or behavioral issues, and facial differences.
Learn more about 22q11.2 Deletion Syndrome (DiGeorge Syndrome)
Alagille Syndrome
Condition
Alagille syndrome causes progressive destruction of the bile ducts.
Aortic Valve Stenosis
Condition
Aortic valve stenosis is a narrowing of the aortic valve that can stop blood from flowing properly out of the heart.
Arrhythmogenic Cardiomyopathy
Condition
Arrhythmogenic cardiomyopathy is a condition when heart rhythm disturbances precede the classical changes in the heart muscle seen in cardiomyopathy.
Barth Syndrome
Condition
Barth syndrome is metabolic disorder that affects the heart, muscles, immune system, and growth. It almost always occurs in boys.
Birth Defects and Congenital Anomalies
Condition
A birth defect is a health problem or a physical abnormality.
Catecholaminergic Polymorphic Ventricular Tachycardia
Condition
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited cardiac condition that causes sudden rhythm disturbances in otherwise healthy children.
Learn more about Catecholaminergic Polymorphic Ventricular Tachycardia
Congenital Heart Defects
Condition
A congenital heart defect is a structural problem of the heart that develops during pregnancy.
Heart Tumor
Condition
A heart tumor, also known as a cardiac tumor, is a rare, abnormal growth that develops in the heart.
Kabuki Syndrome
Condition
Kabuki syndrome is a rare congenital disorder.
Loeys-Dietz Syndrome
Condition
Loeys-Dietz syndrome is a rare, genetic condition that affects the formation of a child’s connective tissue.
Long QT Syndrome
Condition
Long QT Syndrome (LQTS) is an inherited condition that affects the heart’s electrical rhythm and can cause fast, erratic heartbeats.
Marfan Syndrome
Condition
Marfan syndrome is a genetic disorder that causes the body's connective tissues to be weaker than they should be.
Tetralogy of Fallot (TOF) with Pulmonary Atresia
Condition
Tetralogy of Fallot (TOF) with pulmonary atresia is a more severe form of TOF, where the heart’s anatomy prevents enough oxygen-poor (blue) blood from flowing to the lungs to receive oxygen.
Learn more about Tetralogy of Fallot (TOF) with Pulmonary Atresia
Turner Syndrome
Condition
Turner syndrome is a genetic disorder that affects females who have a missing or incomplete X chromosome.
Williams Syndrome
Condition
Williams syndrome is a rare developmental disorder that can affect many parts of the body, including the heart and blood vessels.