Hypertrophic Cardiomyopathy: For Patients, Their Families and Interested Physicians, 2nd Edition

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Format: eBook
Pub. Date: 2008-04-01
Publisher(s): Wiley-Blackwell
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Summary

When there is a diagnosis of HCM in a family, this complete, easy-to-read guide is your essential resource for finding the answers to your many questions. In clear and straightforward language, it explains what hypertrophic cardiomyopathy is, what the symptoms are, and how it can be treated, as well as reviewing the genetic implications and offering candid lifestyle advice. Drawing on the expertise of Dr. Barry Maron, an internationally recognized authority on HCM, the book addresses major questions and concerns of both patients and families. Fully revised to reflect the latest developments, Hypertrophic Cardiomyopathy: For patients, their families and interested physicians, Second Edition, is a valuable source of straightforward advice and dependable information for everyone who is affected by HCM.

Table of Contents

Acknowledgments
Dedication
Foreword
Introduction
What is hypertrophic cardiomyopathy (HCM)?
Historical perspective and names
How common is HCM?
What is the cause of HCM?
Heart structure in HCM
When does HCM develop?: HCM in infants and children
Gender and race
What are the symptoms of HCM?
How is HCM diagnosed and what tests are used?
Other investigations that may be useful
General outlook for patients with HCM
Complications of HCM
Special considerations: Athletes and sports activities
Treatments for HCM
Is a cure available?
Family screening
What about having children?: Pregnancy and delivery
Routine medical care
General lifestyle advice
Support and advocacy groups
What research is being conducted?
The 34 most frequently asked questions by patients about HCM, as
addressed to the HCMA
Glossary
Key HCM References
Appendix
HCMA Membership Application
Index
Table of Contents provided by Publisher. All Rights Reserved.

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