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

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 …

Objective: To highlight the epidemiological characteristics and plot the current mapping of
the sickle cell syndromes in children under 15 years old. Methods: A descriptive study was …

Introduction: Sickle cell syndrome (SCS) represent a real health problem. In this work, we
propose to study the epidemiological and clinical features of 66 patients with SCS. Methods …

Despite the unicity of its genetic mutation, Sickle cell homozygosity presents different clinical
features. Our objectives were to evaluate disease severity in Senegalese patients. Sixty (60) …

Aim: The aim of this study is to investigate some immuno-haematological characteristics of
Nigerian sickle cell disease (SCD) patients in asymptomatic steady state. Material and …

Infection is the main factor of morbidity and mortality in children with sickle cell disease
(SCD). The objective of this study is to determine it's epidemiologic outline in senegalese …

Recurrent and often serious infections are common in sickle cell anaemia. The predisposing
causes are multiple, and immune abnormalities are frequently blamed. In this study, immune …

Background Sickle cell disease is a genetic abnormality involving the haemoglobin.
Although, it is primarily a red cell disorders, the white blood cells and platelets are also …

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 …