Cardiomyopathies in children with inborn errors of metabolism

The paper analyzes the recent literature on cardiomyopathies developing in inborn errors of metabolism. It considers cardiomyopathies as a severe manifestation of primary carnitine deficiency, fatty acid transport and β-oxidation defects, organic acidemias, and lysosomal diseases (including Pompe di...

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Autori principali: I. V. Leontyeva, E. A. Nikolaeva
Natura: Artigo
Lingua:Russo
Pubblicazione: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-04-01
Serie:Rossijskij Vestnik Perinatologii i Pediatrii
Soggetti:
children
cardiomyopathy
cardiac arrhythmias
inborn errors of metabolism
carnitine
fatty acids
lysosomal diseases
diagnosis
Accesso online:https://www.ped-perinatology.ru/jour/article/view/297
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