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Assessment of the relationship between fragmented QRS and cardiac iron overload in patients with beta-thalassemia major

OBJECTIVE: Beta-thalassemia major (TM) is a genetic hemoglobin disorder causing chronic hemolytic anemia. Since cardiac insufficiency and arrhythmias are the primary causes of mortality in such patients, monitoring of cardiac iron load is important in management of the disorder. The purpose of this...

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Detalhes bibliográficos
Publicado no:Anatol J Cardiol
Main Authors: Bayar, Nermin, Kurtoğlu, Erdal, Arslan, Şakir, Erkal, Zehra, Çay, Serkan, Çağırcı, Göksel, Deveci, Burak, Küçükseymen, Selçuk
Formato: Artigo
Idioma:Inglês
Publicado em: Kare Publishing 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5336998/
https://ncbi.nlm.nih.gov/pubmed/25252297
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/akd.2014.5188
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