renal pediatric diseases

Types

 glomerulopathies

• Minimal change disease
• Focal segmental glomerulosclerosis (FSGS)
• Collapsing glomerulopathy
• Autosomal recessive fsgs
• Autosomal dominant familial fsgs
• Congenital nephrotic syndrome
• Finnish type congenital nephrotic syndrome
• Diffuse mesangial sclerosis
• Membranous nephropathy
• Membranoproliferative glomerulonephritis (MPGN)
• Mpgn type I
• Dense deposit disease, mpgn type II
• Mpgn type III
• Acute postinfectious glomerulonephritis
• Subacute bacterial endocarditis-associated glomerulonephritis
• Human immunodeficiency virus-associated nephropathy (HIVAN)
• Iga nephropathy and henoch–schonlein nephritis
• Primary IgA nephropathy (IgAN)
• Henoch–schonlein nephritis (HSN)

 Hereditary basement membrane diseases

• Alport syndrome
• Thin glomerular basement membrane disease
• Nail patella syndrome
• Collagen type III glomerulopathy
• Pierson syndrome

 Other specific glomerulonephritides

• Lupus nephritis
• Anti-glomerular basement membrane antibody mediated glomerulonephritis
• Pauci-immune anca-associated glomerulonephritis
• Thrombotic microangiopathy

 tubulointerstitial nephritis

 renal cystic diseases

• Autosomal dominant polycystic kidney disease (ADPKD)
• Autosomal recessive polycystic kidney disease (ARPKD)
• Glomerulocystic kidney disease (GCKD)
• Nephronophthisis–medullary cystic kidney disease complex (NPH–MCDC)
• Nephronophthisis
• Medullary cystic kidney disease
• Von hippel–lindau-associated renal cysts
• Tuberose sclerosis-associated renal cysts
• Cystic nephroma
• Localized cystic disease
• Simple cortical cysts
• Acquired cystic kidney disease

 developmental renal defects

• Cystic renal dysplasia (multicystic dysplastic kidney)
• Reflux nephropathy
• Renal hypoplasia
• Renal tubular dysgenesis

 Renal transplant pathology

• Donor graft biopsies
• Acute rejection
  -* Acute cellular rejection
• Acute antibody mediated rejection (acute humoral rejection)
• Chronic rejection and chronic allograft nephropathy
• Acute ischemic injury in transplants
• Calcineurin inhibitor toxicity
• Other graft pathologies
• Infective graft complications
• De novo graft glomerulonephritis
• Recurrent diseases
• Post-transplant lymphoproliferative disorder

 Miscellaneous

• Cryoglobulinemic nephropathy
• End stage renal disease
• Paroxysmal nocturnal hemoglobinuria
• Oxalosis (primary hyperoxaluria)

Etiology

 genetic renal diseases
 infectious renal diseases

See also

 Diseases