Sickle cell disease (SCD) is an inherited condition characterized by chronic haemolytic
anaemia. SCD is associated with moderate to severe anaemia, hypercoagulable state and …

It has been well-described that sickle cell disease (SCD) due to HbSS or HbSC is
associated with systemic activation of coagulation. A single study has reported a similar …

Background: Nearly every component of hemostasis is altered in patients with sickle cell
disease (SCD). Though these patients are known to be in hypercoagulable state, increased …

Background: Sickle cell disease (SCD) is considered to be a hypercoagulable state that
contributes to the morbidity associated with the disease. Numerous mechanisms can …

Background: Sickle cell disease (SCD) is an autosomal recessive disorder that is
characterised with chronic anaemia and painful crisis. SCD is associated with …

Background: The evidence from various studies showed that patients with sickle cell disease
(SCD) have altered components of hemostasis such as platelet function, procoagulant …

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 …

Background: Reports from various studies showed that patients with sickle cell anemia
(SCA) have altered components of hemostasis such as platelet function, the procoagulant …

Sickle cell disease (SCD) is a genetic disease characterized by hypercoagulable state and
increased risk of thromboembolic events, a rare but significant complication of SCD. Protein …

Background: We tried to understand whether or not there is an association between platelet
(PLT) and white blood cell (WBC) counts of peripheric blood and severity of sickle cell …