| HVUS | hypocomplementemic vasculitis urticaria syndrome |
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| HUVS | Hypocomplementemic urticarial vasculitis syndrome |
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| hypocomplementemic glomerulonephritis | <pathology> A kidney disorder which results in kidney dysfunction. Inflammation of the glomeruli result from an abnormal immune response and the deposition of antibodies within the kidney (glomerulus) ultrastructure. Membranoproliferative glomerulonephritis has been divided into two different types in the basis of where the antibodies are deposited in the glomerulus. MPGN type I, the more common type, deposits antibodies in the subendothelial layer of the basement membrane, whereas type II deposits antibodies in the bottom layer of the basement membrane. Symptoms include cloudy urine (pyuria), decreased urine output, swelling and hypertension. This disorder often results in end-stage renal disease. Acronym: MPGN (26 Mar 1998) |
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| hypocomplementemic vasculitis | Cutaneous lesions resembling urticaria but lasting more than 24 hours, with biopsy findings of leukocytoclastic vasculitis and variable systemic changes, usually with hypocomplementemia. Synonym: hypocomplementemic vasculitis. (05 Mar 2000) |
| hypocomplementemic |
denoting or involving lowered levels of complement in the blood.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| hypocomplementemic v. |
hypersensitivity vasculitis accompanied by hypocomplementemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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