1) G6PD deficiency
G6PD缺陷症
1.
The hematological study of the thalassemia children accompanied with G6PD deficiency;
地中海贫血合并G6PD缺陷症血液学特点
2) G6PD deficiency
G6PD缺陷
1.
OBJECTIVE To study the methods for early diagnosis of G6PD deficiency and prevention of hyperbiliru-binermia(HB).
目的对新生儿筛查检出的G6PD缺陷与高胆的关系进行临床研究,探讨G6PD缺陷的早期诊断及其高胆的防治方法。
3) G6PD deficiency
G6PD缺乏症
1.
Analysis on G6PD deficiency examination among in paediatric Deptof zhuhai doumen at repreduction-age;
斗门地区育龄人群G6PD缺乏症检测结果分析
2.
Analysis on G6PD deficiency examination among 2399 persons at reproduction-age.;
东莞地区2399例育龄夫妇G6PD缺乏症的筛查结果分析
3.
Detection of the globin gene defect in G6PD deficiency children;
G6PD缺乏症患儿地中海贫基因缺陷的检测
4) G6PD deficiency
G6PD 缺乏症
1.
Results There were 488 patients whose ratio of G6PD/6PGD were abnormal and Incidence of G6PD deficiency is 6.
目的了解广东地区 G6PD 缺乏症的发病情况。
6) G6PD deficiency
G6PD缺乏
1.
The value of the combined tests of thalassemia and G6PD deficiency in detection of before marriage;
地中海贫血和G6PD缺乏联合检测在婚前检查中的价值
2.
Objective To investigate dependability of detecting glucose-6-phosphate(G6PD) activity by biochemistry analyzer for examining G6PD deficiency.
目的探讨在全自动生化仪上直接测定葡萄糖六磷酸盐脱氢酶(G6PD)活性对检测G6PD缺乏的可靠性。
补充资料:5α还原酶缺陷症
5α还原酶缺陷症
病名。亦称不完全型男性假两性畸形Ⅱ型。其缺陷不在于受体,而在于5-α还原酶缺乏,体内双氢睾丸酮不足。为常染色体隐性遗传。病人可有相对正常的内生殖器官,体内有睾丸。但外生殖器官发育障碍,出生时外阴女性化或部分女性化。体型、体态有女性成分,表型为女性。到青春期渐显男性副性征。骨骼粗壮,肌肉较发达,皮下脂肪少,出现喉结,嗓音低沉。但外阴呈女性,有阴裂及盲端阴道,尿道开口于会阴部,体内查不到子宫及输卵管。如性心理为女性,则需在青春期前切除睾丸以避免女性化。嗣后,长期以雌激素替代治疗,可调节为女性。如性心理为男性,则需施手术修复尿道下裂及隐睾。
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