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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Bibliographic Details
Published in:JK Science
Main Authors: Lenaa Sakthiyavathy Manivannan, Kanimozhi Thandapani, Arulkumaran Arunagirinathan
Format: Article
Language:English
Published: Dr. Annil Mahajan 2021-08-01
Subjects:
Sickle beta thalassemia
Hb electrophoresis
HbS
HbF
HbA
Online Access:https://journal.jkscience.org/index.php/JK-Science/article/view/79

Internet

https://journal.jkscience.org/index.php/JK-Science/article/view/79

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