Overview
- Contributions from experts specialized in inherited diseases
- Diagnosis and prevention of the disease aided by colour illustrations
- Includes supplementary material: sn.pub/extras
Access this book
Tax calculation will be finalised at checkout
Other ways to access
Table of contents (26 chapters)
-
Front Matter
-
Sudden Unexplained Death
-
Front Matter
-
-
Arrhythmias and sudden cardiac death. The initial investigation
-
Front Matter
-
Keywords
About this book
Clinical cardiologists are encountering an important challenge in the caring of families with inherited cardiac diseases. The majority of the inherited cardiac diseases causing sudden death express themselves at variable ages in the form of altered muscle function (i.e hypertrophic or dilated cardiomyopathy) or in the form of arrhythmias (i.e. Brugada syndrome, long QT syndrome). However, it is not uncommon that the first sign of the disease may actually be sudden cardiac death, even before the identification of clear clinical abnormalities. In this last decade, with more than 50 new disease-associated genes identified, the possibility of genetic testing has opened a new opportunity to disease diagnosis and prevention. Clinical and genetic research is continuously on-going not only to identify those at risk, but to better define their level or risk still with limited success.
Reviews
Editors and Affiliations
Bibliographic Information
Book Title: Clinical Approach to Sudden Cardiac Death Syndromes
Editors: Ramon Brugada
DOI: https://doi.org/10.1007/978-1-84882-927-5
Publisher: Springer London
eBook Packages: Medicine, Medicine (R0)
Copyright Information: Springer-Verlag London 2010
Hardcover ISBN: 978-1-84882-926-8Published: 14 January 2010
Softcover ISBN: 978-1-4471-6173-8Published: 22 November 2014
eBook ISBN: 978-1-84882-927-5Published: 18 January 2010
Edition Number: 1
Number of Pages: XVI, 340
Topics: Cardiology, Internal Medicine, Emergency Medicine, General Practice / Family Medicine, Sports Medicine, Epidemiology