II. Definition
III. Causes
- See Glomerulonephritis Causes
-
Nephrotic Syndrome
- Minimal Change Disease (NIL Lesion, Lipoid nephrosis)
- Focal Segmental Glomerulosclerosis
- Membranous Glomerulonephritis
- Paraproteinemia (Multiple Myeloma)
- Nephritis with low complement
- Postinfectious proliferative Glomerulonephritis
- Membranoproliferative Glomerulonephritis
- Systemic Lupus Erythematosus
- Cryoglobulinemia
- Diabetes Mellitus
- Hepatitis CVirus
- Nephritis with normal complement
- IgA Nephropathy (Berger's Disease)
- Fibrillary Glomerulonephritis
- Goodpasture's Syndrome
- Rapidly Progressive Glomerulonephritis
- Renal Vasculitis
- Wegner's Granulomatosis
- Polyarteritis Nodosa
V. Symptoms and Signs
VI. Labs: Initial (characterize condition)
- Urine sediment examination
- Proteinuria
- Glomerular Hematuria
- Pigmented or Red Blood Cell Casts
- Dysmorphic Red Blood Cells
- Twenty-four hour urine collection
- Routine blood testing
- Serum chemistries (e.g. Chem8)
- Albumin and Liver Function Tests
- Total Cholesterol
- If over age 40 with Proteinuria >1 gram/24 hours
- Serum Protein Electrophoresis (SPEP)
- Urine Protein electrophoresis
VII. Labs: Next (Screen for etiology)
- Serum Complement (C3, C4, CH50)
- Antinuclear Antibody (ANA)
- Rheumatoid Factor (RF)
- Erythrocyte Sedimentation Rate (ESR)
- Anti-Glomerular Basement Membrane Antibody titer
- Hepatitis Serology (HBsAg, xHBc IgM, HCV)
- Anti-Neutrophilic cytoplasmic Antibody (ANCA)
- Anti-streptolysin O titer (ASO Titer)
- Human Immunodeficiency Virus (HIV)
VIII. Diagnostics
- Renal Ultrasound
- Renal biopsy
IX. Management
- Treat specific cause