Sickle cell syndromes, including sickle cell disease (SCD) and sickle cell trait, are
associated with multiple kidney abnormalities. Young patients with SCD have elevated …

Sickle cell nephropathy is a major complication of sickle cell disease. It manifests in different
forms, including glomerulopathy, proteinuria, hematuria, and tubular defects, and frequently …

The renal features of sickle cell disease (SCD) include some of the most common reasons
for referral to nephrologists, such as hematuria, proteinuria, tubular disturbances and …

Sickle cell disease (SCD) produces many structural and functional abnormalities in the
kidney, including glomerular abnormalities. Albuminuria is the most common manifestation …

Despite its apparently simple molecular aetiology, sickle cell disease (SCD) has long been
known to have a remarkably variable clinical course, with complications involving many …

Sickle cell nephropathy is one of the main chronic complications of sickle cell disease
(SCD), the most common of the hematological hereditary disorders. Several studies have …

Sickle cell disease (SCD) substantially alters renal structure and function, and causes
various renal syndromes and diseases. Such diverse renal outcomes reflect the uniquely …

Renal abnormalities in sickle cell disease. Sickle cell nephropathy is indicated by sickled
erythrocytes, with the consequent effects of decreased medullary blood flow, ischemia …

Introduction: Renal dysfunction is among the most common complication of sickle cell
disease (SCD), from hyposthenuria in children to progression to overt chronic kidney …

This review explores the current model of sickle cell nephropathy and the limitations of the
model. Renal abnormalities are common complications of sickle cell disease (SCD) …