1) 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
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) 17α hydroxylase/17,20 lyase deficiency
17α羟化酶/17,20碳链裂解酶缺陷症
1.
Objective To analyze the clinical and genetic characteristics of 10 Chinese patients with 17α hydroxylase/17,20 lyase deficiency (17OHD).
目的回顾10例17α羟化酶/17,20碳链裂解酶缺陷症(17OHD)患者的资料,分析17OHD的临床特征和分子遗传学特点。
2.
17α hydroxylase/17,20 lyase deficiency (17OHD) is a rare autosomal recessive disorder, characterized by severe hypertension,hypokalemia,sexual infantilism in female, primary amenorrhea, and pseudo hermaphroditism in male.
17α羟化酶/17,20碳链裂解酶缺陷症(17OHD)是先天性肾上腺增生的少见类型。
4) P450c17 enzyme
17α-羟化酶/17,20-碳链裂解酶缺陷症
5) 17α-hydroxylase/17,20 Lyase deficiency
17α-羟化酶/17,20碳链裂解酶缺陷症
1.
Objective To analyze the clinical and molecular genetic characteristics of a patient with 17α-hydroxylase/17,20 Lyase deficiency(17OHD).
目的通过对1例17α-羟化酶/17,20碳链裂解酶缺陷症(17OHD)患者的临床特点和基因突变研究,初步探讨17OHD临床表现的基因分子机制。
6) 11 beta-hydroxylase deficiency
11β-羟化酶缺陷症
1.
Clinical characteristics and treatment of 11 beta-hydroxylase deficiency-report of 9 cases and literature review;
11β-羟化酶缺陷症9例临床特征与治疗分析
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