(Circulation. 2003;108:e133.)
© 2003 American Heart Association, Inc.
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From the Mayo Clinic and Mayo Foundation, Rochester, Minn.
Correspondence to Rick A. Nishimura, MD, Mayo Clinic and Mayo Foundation, 200 First St, SW, Rochester, MN 55905. E-mail jhalling@mayo.edu
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
Affecting approximately one in every 500 people, hypertrophic cardiomyopathy is a unique disease in which there is an abnormal increase in the thickness of the heart muscle. Although the cause of hypertrophic cardiomyopathy was unknown in the past, it is now recognized that people with hypertrophic cardiomyopathy have a gene mutation that causes this abnormality. Most people with hypertrophic cardiomyopathy are relatively asymptomatic and able to maintain a normal lifestyle, but there are some who become severely limited by symptoms of shortness of breath and chest pain. There is also a small number of people with hypertrophic cardiomyopathy who may die suddenly. However, proper diagnosis and treatment of this disorder can relieve symptoms and prolong life.
Abnormalities in Hypertrophic Cardiomyopathy
In people with hypertrophic cardiomyopathy, the muscular wall of the main pumping chamber of the heart (left ventricle) is abnormally thickened (Figure 1). This increased thickness is called hypertrophy, and it usually involves the muscular wall between the right and left ventricles (the ventricular septum), but it may occur in any part of the left ventricle.
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The heart muscle is usually able to pump well despite the hypertrophy, and thus most people do not have limiting symptoms. However, for some people, the thickened heart muscle is abnormally stiff. Therefore, when the left ventricle
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