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. 2009 Nov 12;25(8):1409–1418. doi: 10.1007/s00467-009-1322-7

Table 1.

Classification of membranoproliferative glomerulonephritis

Membranoproliferative glomerulonephritis Associated with systemic and infectious disorders
Idiopathic
  Type I
  Type II (dense deposit disease)
  Type III
Secondary
  Infectious diseases Viral: Hepatitis B and C, human immunodeficiency virus
Bacterial: shunt nephritis, visceral abscesses, infective endocarditis
Protozoal: quartan malaria, schistosomiasis, leprosy
Other: mycoplasma, mycobacteria
  Systemic immune complex diseases Mixed cryoglobulinemia
Systemic lupus erythematosus
Scleroderma
Sjögren’s syndrome
Hereditary deficiencies of complement components
Hypocomplementemic urticarial vasculitis
  Neoplasms Leukemias and lymphomas
Carcinomas
Light-chain disease and plasma cell dyscrasias
  Chronic liver disease Chronic hepatitis
Cirrhosis
  Miscellaneous Partial lipodystrophy
α1-Antitrypsin deficiency
Cystic fibrosis
Drugs (e.g. heroin, α-interferon)
Sarcoidosis
Sickle cell disease
Hemolytic uremic syndrome
Transplant glomerulopathy