Glomerulonephritis causes: Difference between revisions
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==Overview== | ==Overview== | ||
Glomerulonephritis is primarily caused by [[renal]] disease, as well as [[genetic]] disorders and [[hematological]] abnormalities. | |||
==Causes== | ==Causes== | ||
===Common Causes=== | ===Common Causes=== | ||
*[[Churg-strauss syndrome]] | |||
*[[Cryoglobulinaemia]] | |||
*[[Diabetes mellitus type 2]] | |||
*[[Dibasic aminoaciduria type 2]] | |||
*[[Endocarditis]] | |||
*[[Glycogenosis type 1a]] | |||
*[[Henoch-schönlein purpura ]] | |||
*[[Hepatitis b]] | |||
*[[Hereditary onycho-osteodysplasia]] | |||
*[[Hypersensitivity vasculitis]] | |||
*[[Iga nephropathy]] | |||
*[[Lepromatous leprosy]] | |||
*[[Mixed essential cryoglobulinaemia]] | |||
*[[Myeloma]] | |||
*[[Paraneoplastic syndrome]] | |||
*[[Polyarteritis nodosa]] | |||
*[[Radiotherapy]] | |||
*[[Schimke immunoosseous dysplasia]] | |||
*[[Secondary syphilis]] | |||
*[[Serum sickness]] | |||
*[[Sickle cell disease]] | |||
*[[Systemic lupus erythematosus]] | |||
*[[Vasculitis]] | |||
*[[Wegener's granulomatosis]] | |||
*[[Wiskott-aldrich syndrome]] | |||
===Causes by Organ System=== | ===Causes by Organ System=== | ||
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
{{columns-list | {{columns-list| | ||
*[[Alport's syndrome]] | *[[Alport's syndrome]] | ||
*[[Amyloidosis]] | *[[Amyloidosis]] | ||
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[[Category:Needs content]] | [[Category:Needs content]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Organ disorders]] | [[Category:Organ disorders]] | ||
[[Category:Inflammations]] | [[Category:Inflammations]] | ||
[[Category:Kidney diseases]] | [[Category:Kidney diseases]] |
Latest revision as of 21:53, 29 July 2020
Glomerulonephritis Main page |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Luke Rusowicz-Orazem, B.S.
Overview
Glomerulonephritis is primarily caused by renal disease, as well as genetic disorders and hematological abnormalities.
Causes
Common Causes
- Churg-strauss syndrome
- Cryoglobulinaemia
- Diabetes mellitus type 2
- Dibasic aminoaciduria type 2
- Endocarditis
- Glycogenosis type 1a
- Henoch-schönlein purpura
- Hepatitis b
- Hereditary onycho-osteodysplasia
- Hypersensitivity vasculitis
- Iga nephropathy
- Lepromatous leprosy
- Mixed essential cryoglobulinaemia
- Myeloma
- Paraneoplastic syndrome
- Polyarteritis nodosa
- Radiotherapy
- Schimke immunoosseous dysplasia
- Secondary syphilis
- Serum sickness
- Sickle cell disease
- Systemic lupus erythematosus
- Vasculitis
- Wegener's granulomatosis
- Wiskott-aldrich syndrome
Causes by Organ System
Causes in Alphabetical Order
- Alport's syndrome
- Amyloidosis
- Anca vasculitis
- Bacterial endocarditis
- Bucillamine
- C1 esterase inhibitor deficiency
- C2 deficiency
- C4 deficiency
- Chronic hepatitis c
- Churg-strauss syndrome
- Cryoglobulinaemia
- Diabetes mellitus type 2
- Diabetic nephropathy
- Dibasic aminoaciduria type 2
- Endocarditis
- Epstein macrothrombocytopenia syndrome
- Fechtner syndrome
- Focal segmental glomerulosclerosis
- Glycogenosis type 1a
- Gold salts
- Goodpasture's syndrome
- Granulomatosis with polyangiitis
- Henoch-schönlein purpura
- Hepatitis b
- Hereditary nephritis
- Hereditary onycho-osteodysplasia
- Hodgkin's lymphoma
- Hyperdibasic aminoaciduria type 2
- Hypersensitivity vasculitis
- Hypertension
- Hypocomplementemic urticarial vasculitis
- Iga nephropathy
- Indomethacin
- Kartagener's syndrome
- Lepromatous leprosy
- Lithium
- Loiasis
- Lupus
- Lupus nephritis
- Lysinuric protein intolerance
- Malaria
- Membranous nephropathy
- Mercury
- Mixed essential cryoglobulinaemia
- Myeloma
- Nsaids
- Paraneoplastic syndrome
- Parasitic infection
- Penicillamine
- Phenylbutazone
- Polyarteritis
- Polyarteritis nodosa
- Post-streptococcal glomerulonephritis
- Radiotherapy
- Rifampicin
- Scarlet fever
- Schimke immunoosseous dysplasia
- Sebastian platelet syndrome
- Secondary syphilis
- Serum sickness
- Sickle cell disease
- Sjogren's syndrome
- Streptococcal infections
- Systemic lupus erythematosus
- Thin basement membrane disease
- Vasculitis
- Wegener's granulomatosis
- Wiskott-aldrich syndrome