498 top medical experts on IgA Vasculitis across 30 countries and 33 U.S. states, including 404 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- IgA Vasculitis: A systemic non-thrombocytopenic purpura caused by hypersensitivity vasculitis and deposition of IGA-containing immune complexes within the blood vessels throughout the body, including those in the kidney (kidney glomerulus). Clinical symptoms include urticaria; erythema; arthritis; gastrointestinal hemorrhage; and renal involvement. Most cases are seen in children after acute upper respiratory infections.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Vasculitis (2,306), Hemostatic Disorders (360), Immune Complex Diseases (623), Purpura (2,245).
- Synonyms: Allergic Purpura, Anaphylactoid Purpura, Henoch Purpura, Henoch-Schoenlein Purpura, Purpura Hemorrhagica, Nonthrombocytopenic Purpura, Schoenlein-Henoch Purpura, Rheumatoid Purpura, Schoenlein-Henoch Purpura, Hemorrhagic Vasculitis
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