| oxalosis | A genetic disease of autosomal recessive inheritance that results in the deposition of calcium oxalate in the genitourinary system and kidneys (nephrocalcinosis). Usually evident in the first decade of life, progressive renal failure is not uncommon. Inheritance: autosomal recessive. (27 Sep 1997) |
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| primary hyperoxaluria and oxalosis | A metabolic disorder characterised by calcium oxalate nephrocalcinosis and nephrolithiasis, extrarenal oxalosis, and increased urinary output of oxalic and glycolic acids; usually evident clinically in the first decade of life, with progressive renal failure and uraemia; autosomal recessive inheritance. Type I is due to an alteration in alanine:glyoxylate aminotransferase; type II is due to an alteration in d-glycerate dehydrogenase. (05 Mar 2000) |
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| oxalosis |
generalized deposition of calcium oxalate in renal and extrarenal tissues, as may occur in primary hyperoxaluria.
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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