A Rare Hemoglobinopathy Presenting as Chronic Hyperbilirubinemia
Sickle beta thalassemia represents the double heterozygous state of HbS and beta-thalassemia genes. Clinical manifestation varies from those indistinguishable from homozygous sickle cell anemia to completely asymptomatic ones. This disorder is diagnosed by increased levels of HbS, HbF, mildly increa...
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| Formaat: | Boek |
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Dr. Annil Mahajan,
2021-08-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |