Congenital adrenal hyperplasia: basic physiology, clinical presentation and management.

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作者信息

Greger N G, Varma S K

出版信息

Indian J Pediatr. 1987 May-Jun;54(3):303-10. doi: 10.1007/BF02748912.

DOI:10.1007/BF02748912

PMID:3497101

Abstract

摘要

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本文引用的文献

The adrenogenital syndrome with deficiency of 3 beta-hydroxysteroid dehydrogenase.伴有3β-羟类固醇脱氢酶缺乏的肾上腺生殖器综合征

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[The syndrome of male pseudohermaphrodism in congenital adrenocortical hyperplasia without overproduction of androgens (adrenal male pseudohermaphrodism)].先天性肾上腺皮质增生症中无雄激素过度分泌的男性假两性畸形综合征（肾上腺性男性假两性畸形）

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Studies on ACTH action in perfused bovine adrenals: aspects of progesterone as an intermediary in corticosteroidogenesis.

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A pilot newborn screening for congenital adrenal hyperplasia in Alaska.阿拉斯加先天性肾上腺皮质增生症新生儿筛查试点项目。

J Clin Endocrinol Metab. 1982 Sep;55(3):413-20. doi: 10.1210/jcem-55-3-413.

An update of congenital adrenal hyperplasia.

Recent Prog Horm Res. 1981;37:105-81. doi: 10.1016/b978-0-12-571137-1.50008-6.

Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.先天性肾上腺皮质增生症高血压型的新生儿失盐

Pediatrics. 1980 Apr;65(4):777-81.

Salt loss in hypertensive form of congenital adrenal hyperplasia (11-beta-hydroxylase deficiency).先天性肾上腺皮质增生症高血压型（11-β-羟化酶缺乏症）中的盐丢失

J Clin Endocrinol Metab. 1984 Feb;58(2):384-7. doi: 10.1210/jcem-58-2-384.

A heuristic proposal for understanding steroidogenic processes.一种用于理解类固醇生成过程的启发式提议。

Endocr Rev. 1984 Winter;5(1):128-48. doi: 10.1210/edrv-5-1-128.

Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency.21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前治疗。

J Pediatr. 1984 Nov;105(5):799-803. doi: 10.1016/s0022-3476(84)80310-8.

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.类固醇21-羟化酶缺乏症的基因分型：激素参考数据。

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