BACKGROUND β‐Thalassemia is a common hemoglobinopathy in the Arabian Peninsula.
Red blood cell (RBC) transfusion is a cornerstone for its management, but can create …

Background β-Thalassemia is considered one of the common hemoglobin disorders in the
Arabian Peninsula. Red blood cell (RBC) transfusion is a crucial component of the …

Abstract Background and Objective: The mainstay of management of severe β-thalassemia
remains lifelong blood transfusion. The development of one or more alloantibody against …

The development of erythrocyte alloantibodies complicates transfusion therapy in β
thalassemia major patients. These antibodies increase the need for blood and intensify …

BACKGROUND β‐Thalassemia is considered the most common chronic hemolytic anemia
in Egypt. Alloimmunization can lead to serious clinical complications in transfusion …

Context.—Thalassemia is a major health problem in Egypt. Red blood cell alloimmunization
is an important complication in transfusion-dependent patients. Objectives.—To determine …

Severe hemolytic anemia in β-thalassemia major and β-thalassemias/HbE (β-TM) patients
requires giving blood transfusions. Chronic blood transfusions lead to iron overload …

Objective: Frequency of red cell ALLOIMMUNIZATION in patients with b-major-
THALASSEMIA in Mofid children's hospital. Tehran. Iran. Material & Methods: This is a cross …

Background and Objectives Red blood cell alloimmunization is associated with haemolytic
reactions and severe clinical consequences. The rate of alloimmunization in multitransfused …

Background Beta thalassemia is considered a severe, progressive anemia, which needs
regular transfusions for life expectancy. One of the most important complications of regular …