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MORE ABOUT THIS BOOK
Main description:
All physicians practicing medicine encounter patients suffering from cardiovascular disease. This book has been outlined in such a way that vascular surgeons, general internists, neurologists and cardiologists should be able to use it. The book covers the complete scope of cardiac diseases in addition to chapters on hypertension and atherosclerosis. In many patients there is a family history of cerebrovascular accidents, myocardial infarction or peripheral arterial disease. Also in patients reporting collaps, palpitations and arrhythmias the family is crucial and can provide clues to a genetic cause of the disease. This book is published to guide physicians in the process of determining whether a genetic component is likely to be present. Furthermore, information is provided what the possibilities and limitations of DNA diagnostic techniques are. Finally, the importance of newly identified categories of potential patients, i. e. gene carriers without symptoms or any inducible sign of disease, is highlighted. For some patients a genetic diagnosis is essential to determine appropriate therapy and for counseling? In some other diseases DNA diagnostic tools are available but the relevant for the patients may be less clear. In other families the search for a disease causing gene is ongoing and the possibilities to find genes and to unravel the pathophysiology of the disease is limited by the lack of patients. To give insight into the current state of genetic diagnostics, the authors have classified the cardiovascular diseases.
Contents:
List of Contributors. Preface. Introduction to Genetics. 1. Molecular Genetics in Cardiology; M.M.A.M. Mannens, H.J.M. Smeets. 2. Clinical Genetics; J.P. van Tintelen, et al. 3. Genetics of Congenital Heart Disease; P. Grossfeld. Atherosclerosis. 4. Genetics of Hypertension; A.A. Kroon, et al. 5. Lipoproteins and Atherosclerosis; J.C. Defesche, J.J.P. Kastelein. 6. Homocysteine, Genetic Determinants and Cardiovascular Risk; F.F. Willems, et al. 7. Genetic Markers of Hemostatic Factors; D. Girelli, et al. 8. The Pharmacogenetics of Atherosclerosis; J.W. Jukema, W.R.P. Agema. Connective Tissue Disorder. 9. Molecular Diagnosis of the Marfan Syndrome; P.N. Robinson. 10. Williams-Beuren Syndrome ans Supravalvular Aortic Stenosis; L. Perez Jurado. Cardiomyopathy. 11. Mitochondrial Cardiomyopathy; R.J.E. Jongbloed, et al. 12. Hypertrophic Cardiomyopathy; L. Carrier, et al. 13. Dilated Cardiomyopathy; C. Marcelis, et al. Arrhythmias. 14. Idiopathic Ventricular Fibrillation; A.A. Wilde. 15. Diagnosis and Treatment of the Congenital Long QT Syndrome; X.H.T. Wehrens, et al. 16. Atrial Fibrillation; R. Brugada, R. Roberts. 17. Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy; A. Rampazzo, et al. Future of Genetics. 18. Genome Research and Future Healthcare; G.B. van Ommen. Index.
PRODUCT DETAILS
Publisher: Springer
Publication date: October, 2012
Pages: 244
Weight: 411g
Availability: Available
Subcategories: Cardiovascular Medicine, Diseases and Disorders, Genetics, Haematology
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