Nephrotic syndrome classification: Difference between revisions
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* Below table lists different types of nephrotic syndromes:<ref name="pmid10793022">{{cite journal |vauthors=Braden GL, Mulhern JG, O'Shea MH, Nash SV, Ucci AA, Germain MJ |title=Changing incidence of glomerular diseases in adults |journal=Am. J. Kidney Dis. |volume=35 |issue=5 |pages=878–83 |date=May 2000 |pmid=10793022 |doi= |url=}}</ref><ref name="pmid15327377">{{cite journal |vauthors=Heaf J |title=The Danish Renal Biopsy Register |journal=Kidney Int. |volume=66 |issue=3 |pages=895–7 |date=September 2004 |pmid=15327377 |doi=10.1111/j.1523-1755.2004.00832.x |url=}}</ref><ref name=" | * Below table lists different types of nephrotic syndromes:<ref name="pmid10793022">{{cite journal |vauthors=Braden GL, Mulhern JG, O'Shea MH, Nash SV, Ucci AA, Germain MJ |title=Changing incidence of glomerular diseases in adults |journal=Am. J. Kidney Dis. |volume=35 |issue=5 |pages=878–83 |date=May 2000 |pmid=10793022 |doi= |url=}}</ref><ref name="pmid15327377">{{cite journal |vauthors=Heaf J |title=The Danish Renal Biopsy Register |journal=Kidney Int. |volume=66 |issue=3 |pages=895–7 |date=September 2004 |pmid=15327377 |doi=10.1111/j.1523-1755.2004.00832.x |url=}}</ref><ref name="pmid28392820">{{cite journal |vauthors=Ha TS |title=Genetics of hereditary nephrotic syndrome: a clinical review |journal=Korean J Pediatr |volume=60 |issue=3 |pages=55–63 |date=March 2017 |pmid=28392820 |pmc=5383633 |doi=10.3345/kjp.2017.60.3.55 |url=}}</ref> | ||
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Different types of nephrotic syndromes | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |Different types of nephrotic syndromes | ||
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* [[Thrombotic microangiopathy]] | * [[Thrombotic microangiopathy]] | ||
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Hereditary Nephropathy | ! align="center" style="background:#4479BA; color: #FFFFFF;" + |Hereditary Nephropathy | ||
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* [[Alport syndrome]] | * [[Alport syndrome]] | ||
Revision as of 00:53, 29 July 2018
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Nephrotic Syndrome Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Nephrotic syndrome classification On the Web |
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American Roentgen Ray Society Images of Nephrotic syndrome classification |
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Risk calculators and risk factors for Nephrotic syndrome classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Ali Poyan Mehr, M.D. [2]; Associate Editor(s)-in-Chief: Olufunmilola Olubukola M.D.[3] Yazan Daaboul,
Overview
Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology. Primary (idiopathic) nephrotic syndrome is defined as nephrotic syndrome due to a primary glomerular disease. Secondary nephrotic syndrome is defined as nephrotic syndrome due to a primary etiology other than glomerular disorders, such as infections, malignancies, systemic conditions, and medications.
Classification
- Nephrotic syndrome can be classified into primary or secondary depending on the underlying etiology.[1]
| Nephrotic syndrome | |||||||||||||||||||
| Primary | Secondary | ||||||||||||||||||
| Different types of nephrotic syndromes | Disease name | |
|---|---|---|
| Podocytopathies | Primary | Minimal change disease |
| Focal segmental glomerulosclerosis (FSGS) | ||
| Secondary | Infection such as: | |
Drugs/toxins such as:
| ||
| Malignancies such as: | ||
| Genetic disorders such as: | ||
| Membranous glomerulonephritis | Primary | Membranous nephropathy |
| Secondary | ||
| Membranoproliferative glomerulonephritis | Secondary |
|
| Hereditary Nephropathy |
| |
| Glomerular deposition diseases |
| |
| Other lesions | ||
References
- ↑ Kodner C (2009). "Nephrotic syndrome in adults: diagnosis and management". Am Fam Physician. 80 (10): 1129–34. PMID 19904897.
- ↑ Braden GL, Mulhern JG, O'Shea MH, Nash SV, Ucci AA, Germain MJ (May 2000). "Changing incidence of glomerular diseases in adults". Am. J. Kidney Dis. 35 (5): 878–83. PMID 10793022.
- ↑ Heaf J (September 2004). "The Danish Renal Biopsy Register". Kidney Int. 66 (3): 895–7. doi:10.1111/j.1523-1755.2004.00832.x. PMID 15327377.
- ↑ Ha TS (March 2017). "Genetics of hereditary nephrotic syndrome: a clinical review". Korean J Pediatr. 60 (3): 55–63. doi:10.3345/kjp.2017.60.3.55. PMC 5383633. PMID 28392820.