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| Acute Postinfectious Glomerulonephritis.IgA Nephropathy.Hereditary Nephritis ( Alport syndrome)Crescentic Glomerulonephritis.Lupus Nephritis ... |
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| Class IIIA: focal segmental glomerulonephritis (~12% of biopsies); Class IIIB: focalClass V: diffuse membranous glomerulonephritis (~8% of biopsies) ... |
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| PowerPoint Presentation on DEBUT OF SYSTEMIC LUPUS ERITEMATOUS WITH CATASTROPHIC ANTIPHOSPHOLIPID SYNDROME (CAPS): BENEFIT OF THE EARLY TREATMENT or PowerPoint Presentation on Criteria for the diagnosis of CAPS
Disease associations
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| ... gouty arthritis [n = 2], psoriatic arthritis [n = 1], rheumatic fever [n = 1], and systemic lupus erythematosus [n = 1]) acted as controls.1 |
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| Increased renal /systemic vascular resistance ratioaccelerated hypertension, radiation nephritis, scleroderma, systemic lupus erythematosus |
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| (Systemic lupus erythematosus,SLE). ???????????????(Systemic lupus erythematosus, SLE). 15. ???????. IgG????? |
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| ... developing other autoimmune diseases; Examples – Hashimoto’s Thyroiditis, Pernicious Anemia, Insulin-dependant Diabetes, Systemic Lupus Erythemetosus. |
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| Systemic Lupus Erythematosus Cutaneous Tuberculosis (Lupus vulgaris |
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| Nephrotic; Severe nephritis; ARF occassionally ? GFR in ½ . Revised criteria for classification of SLE; Proteinuria >0,5g / day or 3+ Casts – rbc/ granular |
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| Causes of secondary ITP include systemic lupus erythematosus, antiphospholipid antibody syndrome, IgA deficiency, common variable hypogammaglobulinemia, |
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