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  • Book
  • © 2011

Clinical Cardiogenetics

  • Practical cardiac genetics textbook for the clinician
  • Contains detailed information on disease-causing genes
  • Bench-to-bedside approach
  • Includes supplementary material: sn.pub/extras

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Table of contents (28 chapters)

  1. Front Matter

    Pages i-xv
  2. Genetics

    1. Front Matter

      Pages 1-1
    2. Introduction to Molecular Genetics

      • M. M. A. M. Mannens, H. J. M. Smeets
      Pages 3-19
    3. Clinical Genetics

      • J. J. van der Smagt, Peter J. van Tintelen, Carlo L. M. Marcelis
      Pages 21-44
  3. Cardiomyopathy

    1. Front Matter

      Pages 45-45
    2. Hypertrophic Cardiomyopathy

      • Imke Christiaans, Lucie Carrier
      Pages 47-61
    3. Familial Dilated Cardiomyopathy

      • G. Aernout Somsen, G. Kees Hovingh, I. I. Tulevski, Jon Seidman, Christine E. Seidman
      Pages 63-77
    4. Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

      • Moniek G. P. J. Cox, Richard N. W. Hauer
      Pages 79-96
    5. Noncompaction Cardiomyopathy

      • Yvonne M. Hoedemaekers, Kadir Caliskan, Danielle F. Majoor-Krakauer
      Pages 97-122
    6. Mitochondrial Cardiomyopathy

      • N. de Jonge, J. H. Kirkels
      Pages 123-128
    7. Restrictive Cardiomyopathy

      • J. H. Kirkels, N. de Jonge
      Pages 129-139
  4. Primary Electrical Heart Diseases

    1. Front Matter

      Pages 141-141
    2. Congenital Long QT-Syndrome

      • Hubert F. Baars, Jeroen F. van der Heijden
      Pages 143-164
    3. The Brugada Syndrome

      • Begoña Benito, Josep Brugada, Ramon Brugada, Pedro Brugada
      Pages 165-187
    4. Short QT Syndrome

      • Christian Wolpert, Christian Veltmann, Rainer Schimpf, Martin Borggrefe
      Pages 189-196
    5. Catecholaminergic Polymorphic Ventricular Tachycardia

      • Christian van der Werf, Arthur A. M. Wilde
      Pages 197-206
    6. A Molecular Genetic Perspective on Atrial Fibrillation

      • Jason D. Roberts, Michael H. Gollob
      Pages 207-225
  5. Other Hereditary Arrythmias

    1. Front Matter

      Pages 227-227
    2. Idiopathic Ventricular Fibrillation

      • Pieter G. Postema, Christian van der Werf, Arthur A. M. Wilde
      Pages 229-238
    3. The Genetics of Mitral Valve Prolapse

      • Paul L. van Haelst, Toon Oomen, J. Peter van Tintelen
      Pages 239-242

About this book

Clinical management and signs are the focus of this practical cardiogenetic reference for those who are involved in the care for cardiac patients with a genetic disease. With detailed discussion of the basic science of cardiogenetics in order to assist in the clinical understanding of the topic.

The genetic causes of various cardiovascular diseases are explained in a concise clinical way that reinforces the current management doctrine in a practical manner.

The authors will cover the principles of molecular genetics in general but also specific to cardiac diseases. They will discuss the etiology, pathogenesis, pathophysiology, clinical presentation, clinical diagnosis, molecular diagnosis and treatment of each cardiogenetic disease separately. Therapy advice, ICD indications, indications for and manner of further family investigation will all be covered, while each chapter will also contain take-home messages to reinforce the key points. The chapters reviewing the different diseases will each contain a table describing the genes involved in each. Each chapter will also contain specific illustrations, cumulatively giving a complete, practical review of each cardiogenetic disease separately.

Special emphasis will be given to advice on how to diagnose and manage cardiogenetic diseases in clinical practice, which genes should be investigated and why, and the pros and cons of genetic testing. Guidelines for investigation in families with sudden cardiac death at young age will also be included.

This book will be written for the general cardiologist and the clinical geneticist who is involved in cardiac patients and will provide answers to question such as:

Which genes are involved and which mutations? What is the effect of the mutation at cellular level? Which genes should be tested and why? What is the value of a molecular diagnosis? Does it influence therapy? When should the first degree relatives be tested and in which way?

Editors and Affiliations

  • University Medical Centre Utrecht, Utrecht, Netherlands

    H.F. Baars, P.A.F.M. Doevendans, J.J. van der Smagt

Bibliographic Information

  • Book Title: Clinical Cardiogenetics

  • Editors: H.F. Baars, P.A.F.M. Doevendans, J.J. van der Smagt

  • DOI: https://doi.org/10.1007/978-1-84996-471-5

  • Publisher: Springer London

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: Springer-Verlag London Limited 2011

  • Softcover ISBN: 978-1-4471-5703-8Published: 13 December 2014

  • eBook ISBN: 978-1-84996-471-5Published: 25 December 2010

  • Edition Number: 1

  • Number of Pages: XV, 455

  • Topics: Cardiology, Human Genetics, Internal Medicine

Buy it now

Buying options

eBook USD 159.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book USD 209.00
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access