因21-羟化酶部分缺乏所致的先天性肾上腺皮质增生症。五例病例研究。 - Suppr

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超能文献

Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. A study of five cases.

作者信息

Bouchard P, Kuttenn F, Mowszowicz I, Schaison G, Raux-Eurin M C, Mauvais-Jarvis P

出版信息

Acta Endocrinol (Copenh). 1981 Jan;96(1):107-11. doi: 10.1530/acta.0.0960107.

DOI:10.1530/acta.0.0960107

PMID:6257014

Abstract

摘要

相似文献

Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. A study of five cases.因21-羟化酶部分缺乏所致的先天性肾上腺皮质增生症。五例病例研究。

Acta Endocrinol (Copenh). 1981 Jan;96(1):107-11. doi: 10.1530/acta.0.0960107.

"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.伴有21-羟化酶缺乏的“获得性”肾上腺增生与先天性肾上腺增生并非同一遗传疾病。

J Clin Endocrinol Metab. 1979 Feb;48(2):356-9. doi: 10.1210/jcem-48-2-356.

[Partial deficiency in 21-hydroxylase in certain forms of hirsutism].[某些形式多毛症中21-羟化酶部分缺乏]

C R Seances Soc Biol Fil. 1989;183(2):117-21.

Screening heterozygotes for 21-hydroxylase deficiency among hirsute women: lack of utility of the adrenocorticotropin hormone test.

Fertil Steril. 1988 Aug;50(2):228-32. doi: 10.1016/s0015-0282(16)60064-x.

The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).

J Endocrinol Invest. 1984 Apr;7(2):89-92. doi: 10.1007/BF03348395.

Pituitary-adrenal responses to corticotropin-releasing factor in late onset 21-hydroxylase deficiency.迟发型21-羟化酶缺乏症中垂体-肾上腺对促肾上腺皮质激素释放因子的反应

Fertil Steril. 1990 Jul;54(1):79-83. doi: 10.1016/s0015-0282(16)53640-1.

Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Indian J Med Res. 1990 Apr;92:79-82.

The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency.部分性（迟发型）21-羟化酶缺乏症中的下丘脑-垂体-肾上腺轴

J Clin Endocrinol Metab. 1988 Jul;67(1):154-60. doi: 10.1210/jcem-67-1-154.

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.21-羟化酶缺乏所致先天性肾上腺皮质增生症：当前知识综述

J Endocrinol Invest. 1979 Jan-Mar;2(1):93-100. doi: 10.1007/BF03349283.

Serum androgen concentrations in neonates and young infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.21-羟化酶缺乏所致先天性肾上腺皮质增生症新生儿及小婴儿的血清雄激素浓度

Clin Endocrinol (Oxf). 1979 Dec;11(6):575-84. doi: 10.1111/j.1365-2265.1979.tb03111.x.

引用本文的文献

Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study.与先天性肾上腺皮质增生症（CAH）相关的HLA单倍型中CYP21基因的改变：一项家系研究。

Hum Genet. 1993 Aug;92(1):33-9. doi: 10.1007/BF00216142.

The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).

J Endocrinol Invest. 1984 Apr;7(2):89-92. doi: 10.1007/BF03348395.

HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).对5例迟发型21-羟化酶缺乏综合征（21OHDS）患者进行的人类白细胞抗原（HLA）和激素研究。

J Endocrinol Invest. 1986 Feb;9(1):65-70. doi: 10.1007/BF03348067.

Hirsutism: pilosebaceous unit dysregulation. Role of peripheral and glandular factors.多毛症：毛囊皮脂腺单位功能失调。外周因素和腺体因素的作用。

J Endocrinol Invest. 1991 Feb;14(2):153-70. doi: 10.1007/BF03350293.

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