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Home > Art, Film & Photography > Cardiomyopathy: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia, Takotsubo Cardiomyopathy, Peripartum Cardiomyopathy, Dilated Cardiomyopathy
Cardiomyopathy: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia, Takotsubo Cardiomyopathy, Peripartum Cardiomyopathy, Dilated Cardiomyopathy

Cardiomyopathy: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia, Takotsubo Cardiomyopathy, Peripartum Cardiomyopathy, Dilated Cardiomyopathy


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About the Book

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 22. Chapters: Hypertrophic cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Takotsubo cardiomyopathy, Peripartum cardiomyopathy, Dilated cardiomyopathy, Noncompaction cardiomyopathy, Diastolic heart failure, Ventricular remodeling, Restrictive cardiomyopathy, Tachycardia induced cardiomyopathy, Myocytolysis. Excerpt: Hypertrophic cardiomyopathy is a disease of the myocardium (the muscle of the heart) in which a portion of the myocardium is hypertrophied (thickened) without any obvious cause. It is perhaps most well known as a leading cause of sudden cardiac death in young athletes. The occurrence of hypertrophic cardiomyopathy is a significant cause of sudden unexpected cardiac death in any age group and as a cause of disabling cardiac symptoms. Younger people are likely to have a more severe form of hypertrophic cardiomyopathy HCM is frequently asymptomatic until sudden cardiac death, and for this reason some suggest routinely screening certain populations for this disease. A cardiomyopathy is a primary disease that affects the muscle of the heart. With hypertrophic cardiomyopathy (HCM), the sarcomeres (contractile elements) in the heart replicate causing heart muscle cells to increase in size, which results in the thickening of the heart muscle. In addition, the normal alignment of muscle cells is disrupted, a phenomenon known as myocardial disarray. HCM also causes disruptions of the electrical functions of the heart. HCM is most commonly due to a mutation in one of 9 sarcomeric genes that results in a mutated protein in the sarcomere, the primary component of the myocyte (the muscle cell of the heart). While most literature so far focuses on European, American, and Japanese populations, HCM appears in all racial groups. The prevalence of HCM is about 0.2% to 0.5% of the general population. Myosin heavy chain mutati...


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Product Details
  • ISBN-13: 9781155697260
  • Publisher: Books LLC, Wiki Series
  • Publisher Imprint: Books LLC, Wiki Series
  • Height: 246 mm
  • No of Pages: 24
  • Spine Width: 1 mm
  • Weight: 64 gr
  • ISBN-10: 115569726X
  • Publisher Date: 12 Oct 2011
  • Binding: Paperback
  • Language: English
  • Returnable: N
  • Sub Title: Hypertrophic Cardiomyopathy, Arrhythmogenic Right Ventricular Dysplasia, Takotsubo Cardiomyopathy, Peripartum Cardiomyopathy, Dilated Cardiomyopathy
  • Width: 189 mm


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