Hereditary Enzymopathy 遗传性酶病
urea cycle enzymopathy 尿素循环酶病 ; 释义尿素循环酶病
lysosomal enzymopathy 溶酶体酶病
erythrocyte enzymopathy 红细胞酶病
red cell enzymopathy 红细胞酶活性改变
acquired erythrocyte enzymopathy 获得性红细胞酶病
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most frequent genetic enzymopathy, mainly caused by mutations of G6PD gene.
葡萄糖- 6 -磷酸脱氢酶(G6PD)缺乏症是最常见的遗传性酶病，主要由于G6PD基因突变所致。
Objective: To define the prevalence of acquired red cell enzymopathy in leukemia and MDS patients and explore its clinical significance.
目的：调查白血病和骨髓增生异常综合征(MDS)患者红细胞酶和同工酶谱改变的患病率，并研究其临床意义。
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