2024
DOI: 10.1016/j.htct.2023.03.023
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Human leukocyte antigen immunization in transfusion-dependent Moroccan patients with beta-thalassemia major: prevalence and risk factors

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“…Patients with β thalassemia major require regular blood transfusions throughout their lives to maintain haemoglobin levels above 9-10.5 g/dL to suppress ineffective erythropoiesis activity in the bone marrow and prevent growth disorders (Ouadghiri et al, 2023). However, repeated blood transfusions can result in iron overload due to the continuous accumulation of iron, while the body's ability to excrete iron is limited (Ganz & Nemeth, 2023).…”
Section: Introductionmentioning
confidence: 99%
“…Patients with β thalassemia major require regular blood transfusions throughout their lives to maintain haemoglobin levels above 9-10.5 g/dL to suppress ineffective erythropoiesis activity in the bone marrow and prevent growth disorders (Ouadghiri et al, 2023). However, repeated blood transfusions can result in iron overload due to the continuous accumulation of iron, while the body's ability to excrete iron is limited (Ganz & Nemeth, 2023).…”
Section: Introductionmentioning
confidence: 99%