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F-cell levels are altered with erythrocyte density in sickle cell disease

✍ Scribed by Sumanta Basu; Bisnu Prasad Dash; Dilip Kumar Patel; Sudipa Chakravarty; Amit Chakravarty; Debashis Banerjee; Abhijit Chakrabarti


Book ID
116304886
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
229 KB
Volume
47
Category
Article
ISSN
1079-9796

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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

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