1) CYP21 gene
![点击朗读](/dictall/images/read.gif)
21-羟化酶基因
1.
21-hyproxylase is encoded by CYP21 gene.
![点击朗读](/dictall/images/read.gif)
此酶由21-羟化酶基因编码,缺乏可引起皮质醇合成不足以及前体底物堆积。
2) 21-hydroxylase deficiency
![点击朗读](/dictall/images/read.gif)
21-羟化酶缺乏症
1.
Genotype and clinical characteristics of Chinese patients with nonclassical steroid 21-hydroxylase deficiency;
非经典型21-羟化酶缺乏症基因型和临床特征
2.
The major cause of CAH is 21-hydroxylase deficiency (21-OHD), which accounts for 90%~95% of all cases in most populations.
目的: 21-羟化酶缺乏症(21-hydroxylase deficiency,21-OHD)是先天性肾上腺皮质增生症(congenital adrenal hyperplasia,CAH)中最常见的一种类型,属于常染色体隐性遗传性疾病。
3) 21 hydroxylase deficiency
![点击朗读](/dictall/images/read.gif)
21羟化酶缺陷症
1.
Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level.
目的分析19例21羟化酶缺陷症(21OHD)患者的临床和随访资料,提高该病的诊断和治疗水平。
4) 21-hydroxylase deficiency
![点击朗读](/dictall/images/read.gif)
21-羟化酶缺乏
1.
Objective To evaluate the diagnosis and treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency.
目的探讨21-羟化酶缺乏(21-hydroxylasedeficiency,21-OHD)致女性假两性畸形的临床诊断及治疗方法。
5) steroid 21-hydroxylase (CYP21)
![点击朗读](/dictall/images/read.gif)
类固醇21-羟化酶
补充资料:21-羟化酶缺陷
21-羟化酶缺陷
表现为失盐型,因盐皮质激素的合成受阻而肾脏无法保钠,出现低钠血症,表现为纳差、严重呕吐、脱水,以致威胁生命。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条