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Pediatr Transplant ; 19(4): E93-6, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25758207

ABSTRACT

Iron overload cardiomyopathy secondary to ß-thalassemia major is a potentially reversible condition managed with chelation and medical hemodynamic support, as bridge-to-recovery or transplant. We describe our experience, and challenges faced, in a pediatric patient with iron overload cardiomyopathy secondary to ß-thalassemia major, requiring biventricular MCS.


Subject(s)
Shock, Cardiogenic/etiology , beta-Thalassemia/therapy , Adolescent , Cardiomyopathies/etiology , Cardiomyopathies/therapy , Chelating Agents/therapeutic use , Female , Heart Transplantation , Heart-Assist Devices/statistics & numerical data , Hemodynamics , Humans , Iron Overload/etiology , Iron Overload/therapy , Radiography, Thoracic , Shock, Cardiogenic/therapy , beta-Thalassemia/complications
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