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[丙酮酸激酶缺乏症的诊断]

[Diagnosis of pyruvate kinase deficiency].

作者信息

Illum N O

机构信息

børneafdeling GGK, Rigshospitalet, København.

出版信息

Ugeskr Laeger. 1995 Apr 10;157(15):2160-1.

PMID:7652957
Abstract

Two children with nonspherocytic anaemia and pyruvate kinase deficiency had their diagnosis delayed due to normal initial estimations of enzyme activity. Repeated analyses involving other glycolytic enzymes documented an increased glucose-6-phosphate dehydrogenase activity as a function of high reticulocyte counts. The pyruvate kinase activity showed subnormal values. By simple comparison of both enzyme activities a true pyruvate kinase activity of below 50% was estimated thus rendering the diagnosis of pyruvate kinase deficiency highly probable. Analyses of more than one glycolytic enzyme should be performed in young children with otherwise unexplained haemolysis and associated high reticulocyte counts.

摘要

两名患有非球形细胞性贫血和丙酮酸激酶缺乏症的儿童,因其酶活性的初始估计值正常,诊断被延迟。涉及其他糖酵解酶的重复分析表明,葡萄糖-6-磷酸脱氢酶活性随着网织红细胞计数升高而增加。丙酮酸激酶活性显示低于正常水平。通过简单比较这两种酶的活性,估计丙酮酸激酶的实际活性低于50%,从而使丙酮酸激酶缺乏症的诊断极有可能。对于患有不明原因溶血且伴有高网织红细胞计数的幼儿,应进行不止一种糖酵解酶的分析。

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