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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: I. V. Leontyeva, E. A. Nikolaeva
Materyal Türü: Artigo
Dil:Russo
Baskı/Yayın Bilgisi: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-04-01
Seri Bilgileri:Rossijskij Vestnik Perinatologii i Pediatrii
Konular:
children
cardiomyopathy
cardiac arrhythmias
inborn errors of metabolism
carnitine
fatty acids
lysosomal diseases
diagnosis
Online Erişim:https://www.ped-perinatology.ru/jour/article/view/297
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller