Abstract Background Thalassemia is the most prevalent single-gene disorder. Myocardial and hepatic iron depositions lead to complications and eventually death. We aimed to assess the diagnostic efficacy of magnetic resonance imaging T2* (MRI T2*) in quantifying iron overload in liver and heart in transfusion-dependent B-thalassemia major (TDT) children. Methods Prospective clinical study was carried on sixty children diagnosed with TDT. All of them underwent laboratory investigations, including CBC, serum iron, and ferritin levels. MRI T2* of the heart and liver was carried out to measure the iron overload and estimate the left ventricular ejection fraction (LVEF). Results Thirty-eight males and 22 females with TDT with a mean age of 13.23 ...
Extremely diverse phenotypes exist within the homozygous and compound heterozygote states for \u3b2-...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
Myocardial disease remains the life-limiting complication of thalassaemia major (TM). In this study,...
Objective This study was performed to assess cardiac and hepatic iron overload in young patients wit...
Background: Cardiac failure secondary to transfusional iron overload is the most common cause of dea...
The patients of thalassaemia major need repeated blood transfusion which leads to excess iron deposi...
Iron can be deposited in all internal organs, leading to different types of functional abnormalities...
Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to severe an...
Background—Cardiovascular magnetic resonance (CMR) plays a key role in the management of thalassemia...
AbstractPatients with chronic hemolytic anemia like thalassemia and sickle cell anemia need repeated...
Objectives: To evaluate the use of magnetic resonance imaging inpatients with β-thalassemia and to c...
Aim of the study: The aim of this study was to assess the utility of MRI as a non-invasive technique...
Background: routine blood transfusion in transfusion-dependent-thalassemia (TDT) causes iron accumul...
Background Routine blood transfusions and increased intestinal iron absorption lead to iron accumula...
Introduction: In this study, we aimed to assess the relationship of cardiac and hepatic T2* magnetic...
Extremely diverse phenotypes exist within the homozygous and compound heterozygote states for \u3b2-...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
Myocardial disease remains the life-limiting complication of thalassaemia major (TM). In this study,...
Objective This study was performed to assess cardiac and hepatic iron overload in young patients wit...
Background: Cardiac failure secondary to transfusional iron overload is the most common cause of dea...
The patients of thalassaemia major need repeated blood transfusion which leads to excess iron deposi...
Iron can be deposited in all internal organs, leading to different types of functional abnormalities...
Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to severe an...
Background—Cardiovascular magnetic resonance (CMR) plays a key role in the management of thalassemia...
AbstractPatients with chronic hemolytic anemia like thalassemia and sickle cell anemia need repeated...
Objectives: To evaluate the use of magnetic resonance imaging inpatients with β-thalassemia and to c...
Aim of the study: The aim of this study was to assess the utility of MRI as a non-invasive technique...
Background: routine blood transfusion in transfusion-dependent-thalassemia (TDT) causes iron accumul...
Background Routine blood transfusions and increased intestinal iron absorption lead to iron accumula...
Introduction: In this study, we aimed to assess the relationship of cardiac and hepatic T2* magnetic...
Extremely diverse phenotypes exist within the homozygous and compound heterozygote states for \u3b2-...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
Myocardial disease remains the life-limiting complication of thalassaemia major (TM). In this study,...