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Acute hemolysis due to G6PD deficiency occurred in two of the children. 合并葡萄糖六磷酸酶缺乏症而导致溶血的有2个小孩。
Possibly IVS 11 T93C mutation is of non African origin. IVS 11 T93C and C1311T might jointly result in G6PD deficiency. IVS- 11T93C突变可能起源于非洲以外地区 ,并与 C1311T共同作用而导致 G6 PD活性降低。
It is believed to be important in the pathogenesis of favism, the haemolytic anaemia in G6PD deficiency. 本人近年来发现在睡眠时会磨牙，有时我自己会知道，有时则不知，为何会如此？
Methods: Using NBT paper strip method to screen and G6PD/6PGD ratio quantitative NBT method to confirm G6PD deficiency. 其基本病因是由于G6PD基因点突变，造成G6PD亚基个别氨基酸替换，从而造成酶活性减低，病人出现临床症状。
Patients with G6PD deficiency are at risk of hemolytic anemia in states of oxidative stress. 当G6PD患者的氧化反应转趋剧烈便有可能出现溶血性贫血现象；
Objective: To investigate the frequency of G6PD deficiency gene in the Yao nationality in Libo county, Guizhou. 目的:调查贵州省荔波县瑶族葡萄糖-6-磷酸脱氢酶(G6PD)缺陷症的基因频率。
Objective The frequency of G6PD deficiency in the Tujia nationality in Jiangkou,Guizhou was investigated. 目的调查贵州省江口土家族男性葡萄糖-6-磷酸脱氢酶(G6PD)缺陷症的基因频率。
Conclusion There is a high incidence of G6PD deficiency in Tujia nationality in Jiangkou,Guizhou.The inves... 为该地区预防该疾病、指导临床、提高少数民族的素质及研究该民族起源提供了一定的依据。
Conclusion： There is a remarkable relationship between the degree of the G6PD deficiency and the incidence of hyperbilirubinemia. 结论：G6PD活性缺乏程度与患儿高胆红素血症的发生率有显著的相关性。
Objective:Analysing information of neonatal screening in Huizhou city to investigate the morbidity of PKU,CH and G6PD deficiency. 目的:了解惠州市新生儿PKU、CH、G6PD缺陷的发病率及新生儿疾病筛查的情况。
Results:The activity of G6PD was increased significantly in malignant lymphoma( P <0.01),G6PD deficiency was increased significantly ( P <0.05). 结果:与正常人相比恶性淋巴瘤G6PD活性显著增高(P<0。01);G6PD缺乏率显著增高(P<0。
Should the name listed in both cards be the same?Where can I can a full list of medicine the a G6PD deficiency patient should be avoided ? 她的举动不会伤害他人，只会伤害自己，总之无论甚麽程况底下，总是喜欢拔掉自己的头发，但是她的情绪没有任何问题。
The incidence of G6PD deficiency among Dai people is 0.2500 and that among Jinuo people is 0.1395, while the later has a frequency of 0.1579 with defect in the G6PD gene. 经筛查发现西双版纳州傣族及基诺族G6PD缺乏症的患病率分别为0.;2500和0
Some couples may have family history of genetic diseases like Albinism, Haemophilia, G6PD deficiency or Colour blindness.Tests on genetics may therefore be performed. 伴侣可进行基因测试，以检查是否拥有家族性遗传病的基因，如白化症、血友病、葡萄糖六磷酸去氢酶缺乏症或色盲。
Objective:To study the rate of the combined tests of thalassemia and G6PD deficiency in detection of before marriage,to direct aristogenesis and good brood. 目的探讨地中海贫血和G6PD缺乏联合检测在婚前检查中的发病率,并指导优生优育。方法应用地中海贫血一管筛查法和G6PD比值法检测4268对婚前男女的地中海贫血和G6PD缺乏。
The gene frequency of G6PD deficiency was 0.085 7.Conclusions: There is a high incidence of G6PD deficiency in Yao nationality in Libo county.The investigation resu... 结果:对贵州省荔波县280名瑶族男性进行筛查,共检出24例阳性,其基因频率为00857。
Research of G6PD gene mutation types may provide some useful data for clinical diagnosis and prevention of G6PD deficiency , and for human genetic study. G6PD基因突变类型的研究,为该病的诊断和预防以及人类遗传学研究提供更多的资料和手段。
Abstract: Objective： To study the effect of glucose -6 phosphate dehydrogenate （G6PD） deficiency and hemolytic disease of the newborn （HDN） on the morbidity of hypelbilirubinemia among neonates. 文章摘要: 目的：探讨存在葡萄糖6磷酸脱氢酶（G6PD）缺乏和新生儿溶血病（HDN）双重病因对新生儿高胆红素血症发生率的影响。
Conclusion： In the dual G6PD deficiency and HDN patient - infants, the ratio of the wrecked erythrocyte is higher and the possibility of developing hyperbilirubinemia is much more. 结论：存在G6PD缺乏和HDN双重病因的患儿红细胞溶血破坏的几率增高，其发生高胆红素血症的可能性更大。
Blood transfusion is an important symptomatic measure, as the transfused red cells are generally not G6PD deficient. 由于患者接受输血时，所输之血液并不会有G6PD缺失的情况，故此输血是病发时的有效方法。