Teen dilated cardiomyopathy


Excessive use of alcohol, contact with certain toxins, complications from AIDS, and the use of some therapeutic drugs i. The following are the most common symptoms of restrictive cardiomyopathy. Dilated cardiomyopathy DCM occurs when disease affected muscle fibers are enlarged or stretched dilated in one or more chambers of the heart. But most get medical care only after they show symptoms of heart failure, such as:. This condition occurs rarely in children. For specific medical advice, diagnoses, and treatment, consult your doctor. Children with HCM are also at an increased risk of arrhythmias and sudden cardiac arrest.
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Cardiomyopathy and Your Child

Arrhythmogenic Right Ventricular Cardiomyopathy ARVC Also known as arrhythmogenic right ventricular dysplasia, right ventricular dysplasia, right ventricular cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy ARVC is a very rare condition, and almost unheard of in children. Other forms of hypertrophy are symmetric ventricular hypertrophy thickening is evenly distributed throughout the ventricle including the septum and wall and apical hypertrophy thickening is localized at the bottom portion of the heart. Left ventricular non-compaction LVNC is a rare form of cardiomyopathy that is diagnosed by the presence of excessive deep grooves trabecular recesses in the muscle wall of the lower chambers ventricles of the heart. Cardiomyopathy is a serious disease. Eventually, the blood flow to the heart is restricted.
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ABOUT THE DISEASE

It can run in families. Viral infections that infect the heart are a major cause of cardiomyopathy. This abrupt loss of organized heart function leads to insufficient blood being pumped to the body. This is the most common form of cardiomyopathy and it affects about 6 per million children each year. Left Ventricular Non-Compaction Cardiomyopathy LVNC Also known as isolated non-compaction of the left ventricular myocardium or spongiform cardiomyopathy Left ventricular non-compaction LVNC is a rare form of cardiomyopathy that is diagnosed by the presence of excessive deep grooves trabecular recesses in the muscle wall of the lower chambers ventricles of the heart. When someone is diagnosed with cardiomyopathy, his or her close family members may need to be tested to see if they also have it. But most get medical care only after they show symptoms of heart failure, such as:.
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Description:There have been reports of specific gene mutations associated with LVNC, and the condition has been detected in patients who have generalized skeletal muscle weakness and other signs of neuromuscular or metabolic disorders. Dilated cardiomyopathy DCM occurs when disease affected muscle fibers are enlarged or stretched dilated in one or more chambers of the heart. The condition typically begins in the walls of the heart's lower chambers ventricles , and in more severe cases also affects the walls of the upper chambers atria. Cardiomyopathy is the most common reason for heart transplants in children and teens. This number excludes the increasing number of children with secondary cardiomyopathy and the large pool of undiagnosed, asymptomatic cases. Blood Clots With dilated cardiomyopathy, the blood flow through the heart is abnormal which may cause blood clots to form within the heart thromboembolism. Children with hypertrophic cardiomyopathy may have symptoms that increase with exertion or symptoms may be unpredictable.

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