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遗传性非球形细胞溶血性贫血和己糖激酶缺乏症。

Hereditary nonspherocytic hemolytic anemia and hexokinase deficiency.

作者信息

Beutler E, Dyment P G, Matsumoto F

出版信息

Blood. 1978 May;51(5):935-40.

PMID:638252
Abstract

An 11-yr-old child with mild chronic hemolytic anemia was found to have decreased red cell hexokinase activity in spite of the reduced mean age of her red cell population. Similar decreases in red cell hexokinase activity were documented in the patient's parents and in one sib. The red cells were morphologically normal. Red cell 2,3-DPG levels were normal and ATP and glucose-6-phosphate levels were diminished. The kinetic properties, electrophoretic mobility, and thermal stability of the residual red cell hexokinase were normal or nearly so. Glucose consumption of the hexokinase-deficient cells was not appreciably decreased, probably because less of the potent inhibitor glucose-6-phosphate was present in the erythrocytes. It is likely, although not certain, that in this patient nonspherocytic hemolytic anemia resulted from hexokinase deficiency.

摘要

一名11岁患有轻度慢性溶血性贫血的儿童,尽管其红细胞群体的平均年龄降低,但仍发现其红细胞己糖激酶活性降低。在该患者的父母和一个兄弟姐妹中也记录到了类似的红细胞己糖激酶活性降低情况。红细胞形态正常。红细胞2,3 -二磷酸甘油酸水平正常,而三磷酸腺苷和6 -磷酸葡萄糖水平降低。残余红细胞己糖激酶的动力学特性、电泳迁移率和热稳定性正常或接近正常。己糖激酶缺乏的细胞的葡萄糖消耗没有明显减少,可能是因为红细胞中存在的强效抑制剂6 -磷酸葡萄糖较少。虽然不能确定,但很可能该患者的非球形细胞溶血性贫血是由己糖激酶缺乏引起的。

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