“…Sickle cell disease (SCD) is an inherited hemoglobinopathy that can cause major systemic complications. 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 During hypoxia, the defective haemoglobin causes erythrocyte deformity, which consequently creates vaso-occlusive crisis and causes significant pain, the leading cause of SCD hospitalisation. 1 , 4 , 16 SCD negatively impacts the cardiovascular, respiratory, gastrointestinal, renal, neurologic, ocular and skeletal systems.…”