Pediatric cardiomyopathy: importance of genetic and metabolic evaluation

BACKGROUND: Cardiomyopathy is a heterogeneous disease with a strong genetic component. A research-based pediatric cardiomyopathy registry (PCMR) identified familial, syndromic, or metabolic causes in 30% of children. However, these results pre-dated clinical genetic testing. METHODS AND RESULTS: We...

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Bibliografiske detaljer
Main Authors:	Kindel, Steven J., Miller, Erin M., Gupta, Resmi, Cripe, Linda H., Hinton, Robert B., Spicer, Robert L., Towbin, Jeffrey A., Ware, Stephanie M.
Format:	Artigo
Sprog:	Inglês
Udgivet:	2012
Fag:	Article
Online adgang:	https://ncbi.nlm.nih.gov/pmc/articles/PMC3345128/ https://ncbi.nlm.nih.gov/pubmed/22555271 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cardfail.2012.01.017
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Pediatric cardiomyopathy: importance of genetic and metabolic evaluation

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