Oral and maxillofacial sequelae of sickle cell crises in a rare sickle cell disease genotype – HBS/β +-thalassemia
Introduction: Haemoglobin sickle-beta thalassemia (HbS/β-thalassemia) is a rare variant of sickle cell disease (SCD) occurring when both HbS and β-thalassemia genes are inherited. The severity of the condition depends on…