婴儿期草酸中毒
Oxalosis in infancy.
作者信息
Morris M C, Chambers T L, Evans P W, Malleson P N, Pincott J R, Rose G A
出版信息
Arch Dis Child. 1982 Mar;57(3):224-8. doi: 10.1136/adc.57.3.224.
Abstract
We describe 3 infants with nephrocalcinosis and terminal renal failure. In all 3 there was widespread oxalate deposition: biochemical evidence of primary hyperoxaluria was sought but the presence of severe renal failure and the lack of established normal values for urinary and plasma oxalate and glycollate in infants made this diagnosis difficult to establish.
摘要
我们描述了3例患有肾钙质沉着症和终末期肾衰竭的婴儿。在所有3例中均存在广泛的草酸盐沉积：我们寻找原发性高草酸尿症的生化证据，但由于婴儿存在严重肾衰竭，且缺乏尿和血浆草酸盐及乙醇酸盐的既定正常值，使得这一诊断难以确立。
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本文引用的文献
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An unusual case of calcium oxalate deposits in the kidney of a young infant.
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Oxalosis; report of a case with review of the literature.
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PRIMARY HYPEROXALURIA.原发性高草酸尿症
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Oxalosis.草酸中毒
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Ophthalmic manifestations of primary oxalosis.原发性草酸盐沉着症的眼部表现。
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The variation of urinary oxalate excretion with age.尿草酸排泄量随年龄的变化。
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Plasma level and renal clearance of oxalate in normal subjects and in patients with primary hyperoxaluria or chronic renal failure or both.
Clin Sci (Lond). 1979 Apr;56(4):299-304. doi: 10.1042/cs0560299.
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Primary oxalosis: clinical and biochemical response to high-dose pyridoxine therapy.
Metabolism. 1979 May;28(5):542-8. doi: 10.1016/0026-0495(79)90195-1.
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