Nephritic syndrome causes: Difference between revisions
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== Causes == | == Causes == | ||
Nephritic syndrome causes are usually grouped into 'focal proliferative' and 'diffuse proliferative' on the basis of [[histology]] (obtained by a renal biopsy). | Nephritic syndrome causes are usually grouped into 'focal proliferative' and 'diffuse proliferative' on the basis of [[histology]] (obtained by a renal biopsy). | ||
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{{WS}} | {{WS}} | ||
[[Category:Needs content]] | [[Category:Needs content]] | ||
[[Category: | [[Category:Disease]] | ||
[[Category:Nephrology]] | [[Category:Nephrology]] | ||
[[Category:Syndromes]] | [[Category:Syndromes]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
Revision as of 14:06, 2 January 2013
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Causes
Nephritic syndrome causes are usually grouped into 'focal proliferative' and 'diffuse proliferative' on the basis of histology (obtained by a renal biopsy).
Focal proliferative
- IgA nephropathy
- chronic liver failure
- Celiac sprue
- dermatitis herpetiformis
- Henoch-Schoenlein purpura
- Alport syndrome
- SLE
Diffuse proliferative
- focal glomerulosclerosis
- membranoproliferative glomerulonephritis (malaria, hepatitis B, hepatitis C, chronic infection, sickle-cell disease, SLE, hemolytic uremic syndrome / thrombotic thrombocytopenic purpura)
- cryoglobulinemia
- SLE
- rapidly progressing glomerulonephritis (RPGNs) - several.