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A person with Beta Thalassemia Major is completely transfusion dependent from about 6-24 months of age requiring 2-4 units of blood every 15-30 days for survival apart from complex iron chelation to control the excess iron deposition due to the repeated blood transfusions and increased iron absorption caused by this ineffective red blood cell production

Treatment is delivered through a series of injections and may be combined with other regenerative therapies

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Blagosklonny 2009

Therefore, supplements might be beneficial

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