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Genetic and Rare Diseases Information Center (GARD)

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Hemoglobin sickle-beta thalassemia

Other Names for this Disease
  • Hb S beta-thalassemia
  • Sickle beta thalassemia
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  • What is the best pain management regimen for a 50-year-old with hemoglobin sickle-beta thalassemia experiencing sickle cell crisis? Lately, the onset has become more frequent, about every three months. Is this normal? Click here for answer