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Hypertrophic cardiomyopathy

Published online by Cambridge University Press:  13 January 2017

Maully Shah*
Affiliation:
Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America
*
Correspondence to: M. Shah, MBBS, The Cardiac Center, The Children’s Hospital of Philadelphia, 34th and Civic Center Boulevard, Philadelphia, PA 19104, United States of America. Tel: 267 425 6603; Fax: 215 590 1340; E-mail: Shahm@email.chop.edu

Abstract

Hypertrophic cardiomyopathy is a common, inherited heart disease with a heterogeneous clinical presentation and natural history. Recently, advances in diagnosis and treatment options have been instrumental in decreasing the frequency of adverse clinical events; however, complete elimination of sudden cardiac death still remains an elusive gain. This article discusses several aspects of this condition in the young: epidemiology, clinical phenotypes, risk factors, prevention of sudden cardiac death, and risks of athletic participation.

Type
Original Articles
Copyright
© Cambridge University Press 2017 

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