2) 17α-hydroxylase deficiency
17α-羟化酶缺乏症
1.
Molecular genetic study on 17α-hydroxylase deficiency;
17α-羟化酶缺乏症的分子遗传学研究
3) combined 17-alpha-hydroxylase/17,20-lyase deficiency
17α羟化酶/17,20裂链酶联合缺乏
4) 17α-hydroxylase/17,20-lyase deficiency
17α-羟化酶/17,20-裂解酶缺乏症
5) 17α-Hydroxylase Deficiency
17α-羟化酶缺陷症
1.
Clinical Analysis for 9 Patients with 17α-Hydroxylase Deficiency;
17α-羟化酶缺陷症的九例临床分析
6) 21-hydroxylase deficiency
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。
补充资料：17α羟化酶缺乏症
17α羟化酶缺乏症
病名。即17-α羟化酶缺乏综合征。详见该条。
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