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由于红细胞丙酮酸激酶“缺乏”导致的溶血性贫血患者丙酮酸激酶活性升高

Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency".

作者信息

Beutler E, Forman L, Rios-Larrain E

机构信息

Department of Basic and Clinical Research, Research Institute of Scripps Clinic, La Jolla, California 92037.

出版信息

Am J Med. 1987 Nov;83(5):899-904. doi: 10.1016/0002-9343(87)90648-6.

Abstract

Two patients with non-spherocytic hemolytic anemia were found to have elevated red blood cell pyruvate kinase activities commensurate with the decreased mean red cell age, but the residual pyruvate kinase had marked kinetic abnormalities. Accumulation of metabolic intermediates before pyruvate kinase and reduced levels of activity of the red blood cells of the parents of both patients supported the diagnosis of an inherited abnormal pyruvate kinase causing hemolytic anemia. Although it was observed in two unrelated persons, review of enzyme assays performed on the red blood cells of 651 patients with hereditary non-spherocytic hemolytic anemia suggests that this occurrence is rare.

摘要

两名非球形红细胞溶血性贫血患者的红细胞丙酮酸激酶活性升高,与平均红细胞年龄降低相符,但残余的丙酮酸激酶有明显的动力学异常。两名患者父母的红细胞在丙酮酸激酶之前的代谢中间产物积累以及活性水平降低,支持了遗传性异常丙酮酸激酶导致溶血性贫血的诊断。尽管在两名无亲缘关系的个体中观察到了这种情况,但对651例遗传性非球形红细胞溶血性贫血患者红细胞进行的酶分析回顾表明,这种情况很少见。

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