Arrhythmias and Sudden Cardiac Death in Beta-Thalassemia Major Patients: Noninvasive Diagnostic Tools and Early Markers

Beta-thalassemias are a group of inherited, autosomal recessive diseases, characterized by reduced or absent synthesis of beta-globin chains of the hemoglobin tetramer, resulting in variable phenotypes, ranging from clinically asymptomatic individuals to severe anemia. Three main forms have been des...

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Vydáno v:Cardiol Res Pract
Hlavní autoři: Russo, Vincenzo, Melillo, Enrico, Papa, Andrea A., Rago, Anna, Chamberland, Celeste, Nigro, Gerardo
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi 2019
Témata:
Review Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6914907/
https://ncbi.nlm.nih.gov/pubmed/31885907
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/9319832
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