Review Article
Highlights for the Management of a Child with Proteinuria and Hematuria
Table 1
Causes of persistent proteinuria.
| Persistent proteinuria | Glomerular | Tubulointerstitial |
| Diabetes | Acquired | Hypertension | Acute tubular necrosis | Reflux nephropathy | Toxins (gold, lead, copper, and mercury) | Primary glomerulonephropathy conditions | Pyelonephritis | Minimal change nephrotic syndrome | Interstitial nephritis (penicillins and other antibiotics, NSAIDs, and penicillamine) | Focal and segmental glomerulosclerosis | Inherited | Membranous nephropathy | Proximal renal tubular acidosis | Membranoproliferative glomerulonephritis | Cystinosis | Congenital nephrotic syndrome | Galactosemia | Secondary glomerulonephropathy conditions | Lowe syndrome | IgA nephropathy | Dents disease | Infections (Hepatitis B and C, HIV, CMV, malaria, syphilis, streptococcal) | Wilson disease | Henoch-Schönlein nephritis and systemic lupus nephritis (SLE) | Tyrosinemia | Alport syndrome | | Thin basement membrane disease | | Hemolytic uremic syndrome | | Malignancies | | Toxins | |
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Adapted from [8, 9].
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