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Other Names for this Disease
- Idiopathic dilated cardiomyopathy
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 It is the most common type of cardiomyopathy and typically affects those aged 20 to 60. The left ventricle of affected individuals becomes enlarged (dilated) and cannot pump blood to the body with as much force as a healthy heart can. The heart muscle also has difficulty contracting normally, which can lead to irregular heartbeats (arrhythmia), blood clots, or sudden death. Over time, the heart becomes weaker and heart failure can occur. While the cause of dilated cardiomyopathy is often unknown (idiopathic), some cases are acquired or inherited.Dilated cardiomyopathy is a disease of the heart muscle which primarily affects the heart's main pumping chamber, the left ventricle.
Last updated: 9/29/2011
- Dilated cardiomyopathy. MayClinic.com. September 2011; http://www.mayoclinic.com/print/dilated-cardiomyopathy/DS01029/METHOD=print&DSECTION=all. Accessed 9/29/2011.
- What is Cardiomyopathy?. National Heart, Lung and Blood Institute (NHLBI). January 2011; http://www.nhlbi.nih.gov/health/health-topics/topics/cm/types.html. Accessed 9/29/2011.
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- The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Dilated cardiomyopathy. Click on the link to go to OMIM and review these resources.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Dilated cardiomyopathy. Click on the link to view a sample search on this topic.