Clinical Cardiogenetics / edited by Hubert F. Baars, Pieter A. F. M. Doevendans, Arjan C. Houweling, J. Peter van Tintelen.

Format:

Book

Contributor:

Baars, H. F., editor.

Doevendans, Pieter A., editor.

Houweling, Arjan C., editor.

Tintelen, J. Peter van (Johannes Peter), 1964- editor.

SpringerLink (Online service)

Series:

Medicine (Springer-11650)

Language:

English

Subjects (All):

Cardiology.

Human genetics.

Human Genetics.

Local Subjects:

Cardiology.

Human Genetics.

Physical Description:

1 online resource (VIII, 405 pages) : 93 illustrations, 55 illustrations in color

Edition:

Second edition 2016.

Contained In:

Springer eBooks

Place of Publication:

Cham : Springer International Publishing : Imprint: Springer, 2016.

System Details:

text file PDF

Summary:

This extensively revised second edition provides a thorough basic knowledge on the genetic aspects of cardiovascular disorders. Many cardiologists have not been specifically trained in genetics, let alone in explaining genetics to their patients. While clinics for cardiogenetic disorders have been established in many academic teaching hospitals, it is neither desirable nor feasible that the care for this large group of patients and their relatives remains solely restricted to this small number of centers. This book reviews the expertise that all cardiologists, clinical and molecular geneticists, genetic nurses, and social workers need to provide optimal care for individuals with cardiac disease of probable genetic origin and their family members. Clinical Cardiogenetics, Second Edition, compiles the huge amount of information available in a single easy-to-read textbook. It does not require prior expert genetic knowledge and provides a practical clinical primer for cardiologists and other physicians involved in the management of these patients. With the continuing increase in genetic knowledge, and the expanding possibilities to prevent fatal arrhythmias in those individuals at high risk, a steady increase in questions regarding genetics from patients and their relatives in the years to come should be expected. This comprehensive textbook is a valuable tool in dealing with such questions.

Contents:

Molecular Genetics

Clinical genetics

Differential diagnosis of cardiomyopathies

Hypertrophic Cardiomyopathy

Dilated Cardiomyopathy

Arrhythmogenic Cardiomyopathy

Non-Compaction Cardiomyopathy

Hereditary neuromuscular diseases and cardiac involvement

Fabry disease

Long QT Syndrome

Brugada Syndrome

Short QT Syndrome

Cathecholaminergic Polymorphic VT

Sudden death and Idiopathic Ventricular Fibrillation

Thoracic Aortic Aneurysm Dissection

Bicuspid aortic valve

Premature coronary artery disease.

Other Format:

Printed edition:

ISBN:

978-3-319-44203-7

9783319442037

Access Restriction:

Restricted for use by site license.