Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2003;108:e133-e135
doi: 10.1161/01.CIR.0000097621.97566.96
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nishimura, R. A.
Right arrow Articles by Tajik, A.J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nishimura, R. A.
Right arrow Articles by Tajik, A.J.
Related Collections
Right arrow Myocardial cardiomyopathy disease

(Circulation. 2003;108:e133.)
© 2003 American Heart Association, Inc.


Cardiology Patient Page

Hypertrophic Cardiomyopathy

A Patient Perspective

Rick A. Nishimura, MD; Steve R. Ommen, MD; A.J. Tajik, MD

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.


Figure Removed (Available Only in the Full Text)
View larger version (116K):
[in this window]
[in a new window]
 
Figure 1. Schematic diagram of a patient with a normal heart (left) and a patient with hypertrophic cardiomyopathy (right). There is a marked increase in the thickness of the walls of the heart in the patient with hypertrophic cardiomyopathy.

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 . . . [Full Text of this Article]




This article has been cited by other articles:


Home page
CirculationHome page
J. T. Willerson
November 11, 2003
Circulation, November 11, 2003; 108(19): 2291 - 2291.
[Full Text] [PDF]