1) 17α-hydroxylase
17α-羟化酶
1.
Effect of Jinkui Shenqi Pill on 17α-hydroxylase Gene Expression in Kidney Yang Deficiency Rats;
金匮肾气丸对肾阳虚大鼠17α-羟化酶基因表达的影响
2.
Simultaneous Detection of 17α-hydroxylaseand Luteinizing Hormone Receptor( LHR)mRNA from Rat Ovary by Ribonuclease Pro-tection Assay(RPA).;
RNase保护法同时检测黄体生成素受体及17α－羟化酶的mRNA
2) 17α-hydroxylase mRNA
17α-羟化酶mRNA
1.
Study on Relationship of Androgen Receptor mRNA with 17α-hydroxylase mRNA;
小鼠睾丸雄激素受体mRNA与17α-羟化酶mRNA相关性研究
3) 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
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) 17α-hydroxylase/17,20-lyase
17α-羟化酶/17,20碳链裂解酶
1.
Background 17α-hydroxylase/17,20-lyase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia leading to hypokalemic, hypertension and sexual abnormalities such as pseudohermaphroditism in males, and sexual infantilism in females.
17α-羟化酶/17,20碳链裂解酶缺乏症是先天性肾上腺皮质增生症中少见的类型,主要表现为低血钾、高血压及性发育障碍,在男性表现为假两性畸形或外阴女性化,而在女性则表现为第二性征发育障碍。
补充资料：17-羟化酶缺乏综合征
17-羟化酶缺乏综合征
又称“Biglieri综合征”。为常染色体隐性遗传，此酶缺乏致皮质醇和性激素合成障碍。女性青春期缺乏第二性征，原发性闭经，卵巢子宫发育不全，面部皮肤皱纹和早老。男性可出现假两性畸形。由于血浆皮质醇低下，促进ACTH分泌增多，致水钠潴留，高血压、低血钾及低钾性碱中毒。儿童期高血压为主要症状之一。治疗包括糖皮质激素替代治疗及性激素替代治疗。基因型男性(46，XY）而外阴为女性幼稚型者，可手术治疗。
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参考词条