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洛氏综合征及其他肾小管性范科尼综合征病因中蛋白尿的电泳检查

Electrophoretic examination of proteinuria in Lowe's syndrome and other causes of renal tubular Fanconi syndrome.

作者信息

Papadopoulos N M, Costello R, Charnas L, Adamson M D, Gahl W A

机构信息

Clinical Chemistry Service, NICHD, Bethesda, MD 20892.

出版信息

Clin Chem. 1989 Nov;35(11):2231-3.

PMID:2479496
Abstract

Urine samples from 26 patients with five different causes of renal tubular Fanconi syndrome were examined by zone electrophoresis on agarose gel and immunofixation. The tubular disorders associated with Lowe's syndrome, cystinosis, and idiopathic Fanconi syndrome exhibited urine protein electrophoretic characteristics that differentiated them from normal and from each other. In particular, Lowe's syndrome urine exhibited four discrete bands in the gamma globulin zone. Electrophoresis of urinary proteins may be useful in distinguishing among the different metabolic disorders causing renal tubular Fanconi syndrome.

摘要

对26例患有五种不同病因肾小管性范科尼综合征的患者的尿液样本进行琼脂糖凝胶区带电泳和免疫固定检查。与洛氏综合征、胱氨酸病和特发性范科尼综合征相关的肾小管疾病表现出尿液蛋白电泳特征,可将它们与正常情况以及彼此区分开来。特别是,洛氏综合征患者的尿液在γ球蛋白区显示出四条离散条带。尿蛋白电泳可能有助于区分导致肾小管性范科尼综合征的不同代谢紊乱。

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