https://www.selleckchem.com/pr....oducts/sulbactam-piv
BACKGROUND Sickle cell disease (SCD) is a highly prevalent genetic disease worldwide. In the natural evolution of SCD, glomerular lesions can develop, presenting histopathological patterns of segmental or focal membranoproliferative glomerulosclerosis, with or without thrombotic microangiopathy. We report two cases of acute post-infectious glomerulonephritis (APIGN), with atypical presentations, in patients with SCD. CASE PRESENTATION Case 1 An 18-year-old female with SCD presented with a 21-day history of progressive oedema,
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