Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin
Introduction: Delta-beta thalassemia and hereditary persistence of fetal hemoglobin (HPFH) results from a deletion in both the delta and beta genes on chromosome 11. Heterozygous/Homozygous delta-beta thalassemia and HPFH have a varied clinical features including age of presentation, transfusion req...
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| Main Authors: | , , , , |
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| Format: | Book |
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Elsevier,
2023-03-01T00:00:00Z.
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