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Outcomes of Restrictive Cardiomyopathy in Childhood and the Influence of Phenotype
Author(s) -
Steven A. Webber,
Steven E. Lipshultz,
Lynn A. Sleeper,
Minmin Lü,
James D. Wilkinson,
Linda J. Addonizio,
Charles E. Canter,
Steven D. Colan,
Melanie D. Everitt,
John L. Jefferies,
Paul F. Kantor,
Jacqueline M. Lamour,
Renée Margossian,
Elfriede Pahl,
Paolo Rusconi,
Jeffrey A. Towbin
Publication year - 2012
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.112.104638
Subject(s) - medicine , cardiomyopathy , phenotype , restrictive cardiomyopathy , cardiology , pediatrics , heart failure , genetics , biology , gene
Restrictive cardiomyopathy (RCM) has been associated with poor prognosis in childhood. The goal of the present analysis was to use the Pediatric Cardiomyopathy Registry to analyze outcomes of childhood RCM, with a focus on the impact of phenotype comparing pure RCM with cases that have additional features of hypertrophic cardiomyopathy (HCM).

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