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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Detalles Bibliográficos
Autores principales: Bayar, Nermin, Kurtoğlu, Erdal, Arslan, Şakir, Erkal, Zehra, Çay, Serkan, Çağırcı, Göksel, Deveci, Burak, Küçükseymen, Selçuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2015
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336998/
https://www.ncbi.nlm.nih.gov/pubmed/25252297
http://dx.doi.org/10.5152/akd.2014.5188

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336998/
https://www.ncbi.nlm.nih.gov/pubmed/25252297
http://dx.doi.org/10.5152/akd.2014.5188

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