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Primary amenorrhoea with hypertension due to 17-hydroxylase deficiency. Therapy with dexamethasone and ethinyloestradiol.

作者信息

de Lange W E, Weeke A, Artz W, Jansen W, Doorenbos H

出版信息

Acta Med Scand. 1973 Jun;193(6):565-71.

PMID:4721967
Abstract
摘要

相似文献

1
Primary amenorrhoea with hypertension due to 17-hydroxylase deficiency. Therapy with dexamethasone and ethinyloestradiol.17-羟化酶缺乏所致原发性闭经伴高血压。地塞米松和炔雌醇治疗。
Acta Med Scand. 1973 Jun;193(6):565-71.
2
11-beta-hydrosylase deficiency: steroid response to sodium restriction and ACTH stimulation.11-β-羟化酶缺乏症：类固醇对限钠及促肾上腺皮质激素刺激的反应
J Clin Endocrinol Metab. 1972 Aug;35(2):281-7. doi: 10.1210/jcem-35-2-281.
3
[Study of renin activity and aldosterone secretion in adrenal hyperplasia due to 21-hydroxylase deficiency].[21-羟化酶缺乏所致肾上腺增生中肾素活性与醛固酮分泌的研究]
C R Seances Soc Biol Fil. 1969;163(6):1386-90.
4
[Enzyme deficiencies in pathogenesis of hypertension].[酶缺乏在高血压发病机制中的作用]
Union Med Can. 1971 Nov;100(11):2110-5.
5
[The use of cyproteronacetate in patients with adrenogenital syndrome caused by C-21 hydroxylase deficiency].
Orv Hetil. 1974 Oct 20;115(42):2487-90.
6
[Study on the corticosteroids and renin in two children with congenital adrenal hyperplasia due to deficiency of 11- -hydroxylase. Effect of salt restriction and therapy].[11β-羟化酶缺乏所致先天性肾上腺皮质增生症两名患儿的皮质类固醇与肾素研究。限盐及治疗的影响]
Schweiz Med Wochenschr. 1972 Sep 9;102(36):1282-3.
7
[Primary amenorrhea and arterial hypertension in a case of 17 alpha-hydroxylase deficiency].[17α-羟化酶缺乏症一例中的原发性闭经与动脉高血压]
J Gynecol Obstet Biol Reprod (Paris). 1994;23(2):137-40.
8
[Study of renin activity and aldosterone secretion in 7 cases of adrenal hyperplasia due to 21-hydroxylase deficiency].[21-羟化酶缺乏所致肾上腺增生7例肾素活性及醛固酮分泌的研究]
Ann Endocrinol (Paris). 1969 Nov-Dec;30(6):822-30.
9
[Menstruation disorders caused by 17 alpha-hydroxylase deficiency].[17α-羟化酶缺乏所致月经紊乱]
Ned Tijdschr Geneeskd. 1972 Jan 1;116(1):48-50.
10
Study of the level of production of cortisol, corticosterone, aldosterone and deoxycorticosterone in 4 cases of congenital adrenal hyperplasia due to II beta-hydroxylase deficiency.4例因Ⅱβ-羟化酶缺乏所致先天性肾上腺皮质增生症患者皮质醇、皮质酮、醛固酮及脱氧皮质酮生成水平的研究。
Rev Eur Etud Clin Biol. 1971 Jun-Jul;16(6):585-90.

引用本文的文献

1
XY females with enzyme deficiencies of steroid metabolism. A brief review.患有类固醇代谢酶缺乏症的XY女性。简要综述。
Hum Genet. 1980;53(3):291-5. doi: 10.1007/BF00287042.
2
17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.
J Endocrinol Invest. 1991 Feb;14(2):99-108. doi: 10.1007/BF03350278.
3
Canadian Mennonites and individuals residing in the Friesland region of The Netherlands share the same molecular basis of 17 alpha-hydroxylase deficiency.加拿大门诺派与居住在荷兰弗里斯兰地区的个体，在17α-羟化酶缺乏症方面有着相同的分子基础。
Hum Genet. 1992 Apr;89(1):95-6. doi: 10.1007/BF00207050.
4
Deficiency of 17 alpha-hydroxylase associated with absent gonads.17α-羟化酶缺乏伴性腺缺如。
Postgrad Med J. 1992 Jan;68(795):59-61. doi: 10.1136/pgmj.68.795.59.