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Genetic Cardiomyopathies, p. 113-117

DOI: 10.1007/978-88-470-2757-2_10

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The role of clinical observation: red flag 8 - Cardiomyopathies in the first year of life and pediatric cardiomyopathies.

Book chapter published in 2013 by Fulvio Camerini, Enrico Fabris, Rossana Bussani, Gianfranco Sinagra ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Pediatric carduiomyopathies [CMPs] are complex and present challenges to both cardiologists and pediatricians. The incidence of pediatric CMPs is significantly higher in the first year of life than in older age. All types of CMP may be present in early childhood. The most frequent type is dilated cardiomyopathy [DCM], while familial hypetrophic cardiomyopathy [HCM] caused by contractile protein abnormalities usually develops, at least in some series, after the first decade of life.