Non-transfusion-dependent thalassemia (NTDT) has been considered less severe than its
transfusion-dependent variants. The most common forms of NTDT include β-thalassemia …

Beta-thalassemia is a genetic disorder characterized by the impaired synthesis of the
betaglobin chain of adult hemoglobin. The disorder has a complex pathophysiology that …

Background. Thalassemia is a common congenital hemolytic disorder. In severe cases,
regular blood transfusion is essentially required. The role of premedications to prevent …

Background Cardiac complications are important causes of morbidity in patients with
thalassemia intermedia (TI). We aimed to assess left ventricular (LV) function, using new …

Background We aimed to investigate the molecular basis of β-Thalassemia intermedia (TI) in
the West Bank region and its management practices. Methods This was a case series multi …

Background: β thalassemia patients have repeated blood transfusions those lead to iron
overload, resulting in iron toxicity. In such cases Hepcidin results in excessive iron …

Introducción: β-talasemia, es causada por mutaciones en el gen de la globina HBB, que
codifica la subunidad β de la HbA. La enfermedad es conocida por ser altamente prevalente …

Background and objectives: Non-transfusion dependent thalassemia (NTDT) characterized
by an increase iron overload with end-organ damage as a consequence. The aim of the …

Extramedullary hematopoiesis (EMH) is a proliferation of hematopoietic tissue outside the
bone marrow. The most affected areas are paravertebral ones. We report the case of a …

Beta thalassemia is an inherited blood disorder that results in inefficient erythropoiesis due
to genetic mutation that leads to reduction or absence of the hemoglobin beta-globulin …