RT Book, Section A1 Frame, James N. A1 Rodgers, Griffin P. A2 Boyiadzis, Michael M. A2 Frame, James N. A2 Kohler, David R. A2 Fojo, Tito SR Print(0) ID 1128368284 T1 Sickle Cell Disease: Acute Complications T2 Hematology-Oncology Therapy, 2e YR 2016 FD 2016 PB McGraw-Hill Education PP New York, NY SN 9780071637893 LK hemonc.mhmedical.com/content.aspx?aid=1128368284 RD 2024/03/28 AB Individuals are diagnosed with sickle cell disease (SCD) if they have one of several genotypes that result in at least half of their hemoglobin (Hgb) being Hgb S. Sickle cell anemia (SCA) refers to the condition associated with homozygosity for the Hgb S mutation (Hgb SS). Other Hgb mutations may occur with Hgb S causing a similar but milder condition. In SCA, the presence of intracellular hemoglobin S polymerization leads to chronic hemolytic anemia, vasoocclusive crises of varying severity and frequency with cumulative organ damage and systemic manifestations that include impairment in growth and development, susceptibility to infection, and reduced quality and duration of life Segal JB et al. Hydroxyurea for the Treatment of Sickle Cell Disease. Rockville, MD: Agency for Healthcare Research and Quality, 2008 Feb. Report No. 08-E007