Introduction: Thalassemia is the most common genetic disorder worldwide. Regular transfusion therapy, while improving patient quality of life, creates a state of iron overload. Once reticuloendothelial stores saturate, iron deposition increases in parenchymal tissues such as endocrine glands, hepatocytes, and myocardium. Cardiac iron deposition produces arrhythmias, systolic and diastolic dysfunction, and congestive heart failure in the second or third life decade. Aims and Objective: The present study was planned to find the prevalence of thalassemia cardiomyopathy and to study the spectrum of cardiac disease in thalassemia patients. Methods: All consecutive patients of thalassemia more than 12-year-old were included in this study. Screeni...
Background: Frequent blood transfusions lead to various complications in patients with thalassemia m...
Background: To evaluate the use of electrocardiography (ECG) in thalassemia major patients, for the ...
<p><strong>BACKGROUND:</strong> The assessment of cardiac iron overload in thalassemia major has bee...
Background: Paediatric patients with transfusion dependent thalassemia require regular lifelong red ...
Abstract Background and Objective: Many thalassemia patients don't have any symptoms until the dise...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
Beta-thalassemia major is a genetic disorder adversely affecting the life of the patient and the who...
Background: Cardiac iron toxicity is a major cause of mortality in transfusion-dependent beta-thalas...
<p><strong>Introduction: </strong>There are more than 18000 thalassemia patients in Iran. In a curre...
Heart disease remains a leading cause of morbidity and mortality in transfusion-dependent thalassemi...
Background: Thalassemia is an autosomal genetic disease leading to anemia and remains one of the maj...
Introduction: Beta-thalassemia major is the most common chronic hemolytic anemia. It is a well-compr...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
ing relaxation parameter) is abnormally low in approximately 40 % of adults with thalassemia major (...
Aim: to evaluate the relationship between uric acid (UA), hepatic and cardiac iron overload (T2*-MRI...
Background: Frequent blood transfusions lead to various complications in patients with thalassemia m...
Background: To evaluate the use of electrocardiography (ECG) in thalassemia major patients, for the ...
<p><strong>BACKGROUND:</strong> The assessment of cardiac iron overload in thalassemia major has bee...
Background: Paediatric patients with transfusion dependent thalassemia require regular lifelong red ...
Abstract Background and Objective: Many thalassemia patients don't have any symptoms until the dise...
Introduction: Thalassemia is a genetic condition and is one of the commonest single-gene hereditary ...
Beta-thalassemia major is a genetic disorder adversely affecting the life of the patient and the who...
Background: Cardiac iron toxicity is a major cause of mortality in transfusion-dependent beta-thalas...
<p><strong>Introduction: </strong>There are more than 18000 thalassemia patients in Iran. In a curre...
Heart disease remains a leading cause of morbidity and mortality in transfusion-dependent thalassemi...
Background: Thalassemia is an autosomal genetic disease leading to anemia and remains one of the maj...
Introduction: Beta-thalassemia major is the most common chronic hemolytic anemia. It is a well-compr...
Objective: Cardiac T2* magnetic resonance imaging (MRI) has recently attracted considerable attentio...
ing relaxation parameter) is abnormally low in approximately 40 % of adults with thalassemia major (...
Aim: to evaluate the relationship between uric acid (UA), hepatic and cardiac iron overload (T2*-MRI...
Background: Frequent blood transfusions lead to various complications in patients with thalassemia m...
Background: To evaluate the use of electrocardiography (ECG) in thalassemia major patients, for the ...
<p><strong>BACKGROUND:</strong> The assessment of cardiac iron overload in thalassemia major has bee...