A THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA.

Conclusions:Hematological parameters varied with hemoglobin genotype. The C hemoglobin and homozygous alpha thalassemia deletion had better ameliorating effect on SCD hematological parameters than the F hemoglobin in this population. 

Source: Mediterranean Journal of Hematology and Infectious Diseases - January 1, 2022 Category: Hematology Authors: FASOLA ATINUKE Source Type: research