Galand C, Torres M, Boivin P, Bourgeaud J P
Scand J Haematol. 1978 Jan;20(1):77-84. doi: 10.1111/j.1600-0609.1978.tb01557.x.
A new case of glucosephosphate isomerase deficiency with mild haemolytic anaemia was observed in a 6-year-old girl. Deficient enzyme was characterized by a profoundly decreased activity in the red cells, a normal electrophoretic phenotype, normal isoelectric point, normal optimum pH, a molecular instability and a clearly decreased Michaelis constant for fructose-6-phosphate. Propositus was double heterozygote for a 'silent gene' inherited from the mother and an abnormal enzyme from the father. Because this abnormal enzyme has undescribed characteristics, it responds to a new variant for which we propose the name GPI-MYTHO.
在一名6岁女孩中观察到1例新的伴有轻度溶血性贫血的葡萄糖磷酸异构酶缺乏症。缺陷酶的特征为红细胞中活性显著降低、电泳表型正常、等电点正常、最适pH值正常、分子不稳定且对6-磷酸果糖的米氏常数明显降低。先证者是从母亲遗传的“沉默基因”和从父亲遗传的异常酶的双重杂合子。由于这种异常酶具有未描述的特征,它属于一种新的变异型,我们建议将其命名为GPI-MYTHO。