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β-Thalassemia Major (Cooley's Anemia)

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Internal Medicine
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Abstract

β-thalassemia major is a hereditary hemolytic anemia, characterized by deficiency in the hemoglobin beta chain synthesis. Patients with β-thalassemia major are prone to repeated attacks of intravascular hemolysis that requires repeated hospitalization and blood transfusions.

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For Further Reading

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Al-Tubaikh, J.A. (2010). β-Thalassemia Major (Cooley's Anemia). In: Al-Tubaikh, J.A. (eds) Internal Medicine. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-03709-2_56

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  • DOI: https://doi.org/10.1007/978-3-642-03709-2_56

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-03708-5

  • Online ISBN: 978-3-642-03709-2

  • eBook Packages: MedicineMedicine (R0)

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