Burkina Faso belongs to the sicklemic's belt of LEHMAN and is the epicenter of
haemoglobin C. This is the reason of this study on the haematological and biochemical …

Sickle cell disease is an hereditary hemoglobinopathy syndrome which provokes
deglobulization crisis and infectious complications. These infectious diseases may be due to …

Background: Sickle cell anemia a dangerous genetic disorder in which the erythrocytes of
the body caused by a mutation in the HBB gene in the sixth position of the β chain, there is a …

Objectives: Sickle cell disease is an inherited blood disorder caused by abnormal properties
conveyed to sickle cell erythrocyte by mutant sickle cell haemoglobin (Hbs). This study …

Background: Sickle cell anaemia (SCA) is a hereditary disorder associated with high
morbidity and mortality. The objective of this study is to determine the haematological …

Introduction: Sickle cell disease (SCD) is an autosomal inherited structural disorder of
hemoglobin which leads to vaso-occlusive, hematological and infectious crises, including …

Background: There are documented established markers (indices) of disease severity in
patients with sickle cell anemia (SCA) and they determine the course of the disease. This …

Objectives: This study aimed at assessing the clinical features and haematological
parameters in sickler Sudanese patients attending El Obeid Hospitals in North Kordofan …

Introduction: Sickle cell disease is a public health problem in the Republic of Congo where
the prevalence of sickle cell trait is estimated at 1.25%. The objective of this study is to …

Background Effective treatment and management of sickle cell disease (SCD) has been a
challenge in Africa over the years. Hematological parameters are very useful profiles in the …