Osteomyelitis remains one of the greatest risks in orthopaedic surgery. Although many
organisms are linked to skeletal infections, Staphylococcus aureus remains the most …

Sickle cell anemia (SCA), a hereditary blood disorder characterized by the presence of
abnormal hemoglobin, poses a unique set of challenges for both patients and healthcare …

Individuals with sickle cell disease (SCD) and sickle cell trait (SCT) have many risk factors
that could make them more susceptible to COVID-19 critical illness and death compared to …

Sickle cell anaemia (SCD) is a life-threatening haematological disorder which is
predominant in sub-Saharan Africa and is triggered by a genetic mutation of the β-chain …

Independent of etiology, hemolytic diseases are associated with thrombosis, inflammation
and immune dysregulation, all together contributing to organ damage and poor outcome …

Acute chest syndrome (ACS) is a leading cause of respiratory distress and hospitalisation in
children with sickle cell disease (SCD). The aetiology is multifactorial and includes fat …

Sickle cell anemia (SCA) is a hereditary blood disorder characterized by the presence of
abnormal hemoglobin, leading to the deformation of red blood cells and subsequent health …

Maternal hematological disorders during pregnancy may pose a risk to the neurological
development of newborns. To investigate the association between maternal hematological …

Heme is an erythrocyte-derived toxin that drives disease progression in hemolytic anemias,
such as sickle cell disease. During hemolysis, specialized bone marrow-derived …

Significance: Sickle cell disease (SCD) is the most common inherited diathesis affecting
mostly underserved populations globally. SCD is characterized by chronic pain and fatigue …