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 incre...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Dr. Annil Mahajan
2021-08-01
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| Serie: | JK Science |
| Soggetti: | |
| Accesso online: | https://journal.jkscience.org/index.php/JK-Science/article/view/79 |
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