Rahma Guedri

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To the Editor: We presented here the case of a the case of a 9-year-old Tunisian boy with thalassemia major, a second child of consanguineous parents, with a family history of heterozygous b-thalassemia. His disease was primarily manifested by jaundice and splenomegaly. He was diagnosed with homozygous b-thalassemia at the age of 6 months with a stop codon(More)
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