Hypertrophic Cardiomyopathy View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2010

AUTHORS

Frank A. Flachskampf , Ruxandra T. Beyer , Petros Nihoyannopoulos

ABSTRACT

Hypertrophic cardiomyopathy (HCM) is a genetically determined disease with familial and spontaneous occurrence. The disease is often asymptomatic. Symptoms typically develop in young adulthood or later. With advanced disease, the leading symptoms are dyspnea, angina, and syncope. Because of the risk of syncope and of ventricular arrhythmias and sudden death, detection is important even in the absence of symptoms in daily life. On physical examination, the most prominent sign is a systolic murmur over the base of the heart at the left sternal border, which is not transmitted to the carotids. The ECG usually shows signs of left ventricular hypertrophy with strain or left bundle branch block. More... »

PAGES

425-436

Book

TITLE

The ESC Textbook of Cardiovascular Imaging

ISBN

978-1-84882-420-1
978-1-84882-421-8

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-1-84882-421-8_22

DOI

http://dx.doi.org/10.1007/978-1-84882-421-8_22

DIMENSIONS

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