Beta-Thalassemia/Hb E

    Researchedby:
    Brady Holmer
    Last Updated: October 13, 2024

    Hemoglobin E beta-thalassemia is a rare blood disease where an individual inherits the hemoglobin E (HbE) gene from one parent and a gene for beta-thalassemia from another. This disease causes growth retardation, spleen enlargement, and cardiovascular complications.

    examine-databaseExamine Database

    Beta-Thalassemia/Hb E falls under the Cardiovascular Health category.

    21 participants in 1 trial

    Examine Database: Beta-Thalassemia/Hb E

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    Examine Database References

    1. Oxidative Stress Biomarkers - Kalpravidh RW, Siritanaratkul N, Insain P, Charoensakdi R, Panichkul N, Hatairaktham S, Srichairatanakool S, Phisalaphong C, Rachmilewitz E, Fucharoen SImprovement in oxidative stress and antioxidant parameters in beta-thalassemia/Hb E patients treated with curcuminoidsClin Biochem.(2010 Mar)