说明:双击或选中下面任意单词,将显示该词的音标、读音、翻译等;选中中文或多个词,将显示翻译。
您的位置:首页 -> 词典 -> 17α-羟化酶/17,20碳链裂解酶缺陷症
1)  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。
2)  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。
3)  P450c17 enzyme
17α-羟化酶/17,20-碳链裂解酶缺陷症
4)  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。
5)  17α-hydroxylase/17,20-lyase deficiency
17α-羟化酶/17,20-裂解酶缺乏症
6)  combined 17-alpha-hydroxylase/17,20-lyase deficiency
17α羟化酶/17,20裂链酶联合缺乏
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

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