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This thesis investigates the impact of BCL11A single nucleotide polymorphisms on fetal hemoglobin levels and clinical outcomes in sickle cell disease patients in Kassala, Sudan. The study found a predominance of the SS genotype and highlighted the absence of fetal hemoglobin, raising concerns about the underutilization of hydroxyurea treatment. The findings suggest a need for improved management strategies to enhance patient outcomes in sickle cell disease.
- Author
- Hadi Adam
- Language
- EN