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Aggressive medical management according to established protocols for ALF (including treatment of hyperammonemia and detection and management of cerebral edema), with early consideration of apheresis or renal replacement therapy to rapidly remove circulating copper, may stabilize the patient with WD awaiting transplantation

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401 Ferroptosis in thalassemia Thalassemia is a common monogenic inherited disorder primarily caused by a reduction in globin synthesis due to deletion or point mutations of globin gene clusters

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