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F cells, fetal hemoglobin levels, lymphocyte subsets, and frequency of crises in sickle-cell disease in Kuwait

โœ Scribed by S. A. Kaaba; L. Al Fazaa

Publisher
Springer
Year
2000
Tongue
English
Weight
84 KB
Volume
79
Category
Article
ISSN
0939-5555

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Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease
โœ Marcus, Stacy J.; Kinney, Thomas R.; Schultz, William H.; O'Branski, Erin E.; Wa ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 110 KB ๐Ÿ‘ 2 views

Variation in the level of fetal hemoglobin (HbF) accounts for much of the clinical heterogeneity observed in patients with sickle cell disease (SCD). The HbF level has emerged as an important prognostic factor in both sickle cell pain and mortality, and a % HbF of 10-20% has been suggested as a thre