Springer Genetic Cardiomyopathies: A Clinical Approach

This book offers insight on genetics as a primary issue in the diagnosis and management of cardiomyopathies, defining the molecular basis and presenting extensive descriptions of genotype–phenotype correlations. Covers observation, ECG and echocardiography. Review From the reviews:“This is a concise, yet comprehensive review of genetic disorders that lead to inherited cardiomyopathies from internationally respected authorities in this field. … This book is intended for general cardiologists, heart failure/advanced cardiomyopathy cardiologists, pediatric cardiologists, and geneticists. Although it covers a subspecialty topic, it would also benefit medical residents, cardiology fellows, nurse practitioners, physician assistants and medical students with an interest in this field. … The approach of identifying cardiomyopathies based on clinical presentation also makes it an attractive tool for practicing physicians.” (Joaquin Crespo, Doody’s Book Reviews, June, 2013) From the Back Cover In the last decade, genetics has been emerging as a primary issue in the diagnosis and management of cardiomyopathies. This book is intended to be a state-of-the-art monograph on these diseases, describing their genetic causes, defining the molecular basis and presenting extensive descriptions of genotype–phenotype correlations. Other chapters are focused on the role of clinical observation, on ECG and echocardiography. With its highlight on the most recent discoveries in the field of molecular genetics as well as on the correct clinical approach to patients with heart muscle disease, the book is aimed at physicians and clinical cardiologists with a particular interest in myocardial diseases and in their genetic causes.