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Identification of 15 beta-hydroxylated C21 steroids in the neo-natal period: the role of 3 alpha,15 beta,17 alpha-trihydroxy-5 beta-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (CAH) due to a 21-hydroxylase deficiency.

作者信息

Joannou G E

出版信息

J Steroid Biochem. 1981 Sep;14(9):901-12. doi: 10.1016/0022-4731(81)90239-9.

DOI:10.1016/0022-4731(81)90239-9
PMID:6975400
Abstract
摘要

相似文献

1
Identification of 15 beta-hydroxylated C21 steroids in the neo-natal period: the role of 3 alpha,15 beta,17 alpha-trihydroxy-5 beta-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (CAH) due to a 21-hydroxylase deficiency.
J Steroid Biochem. 1981 Sep;14(9):901-12. doi: 10.1016/0022-4731(81)90239-9.
2
Increased urinary excretion of total 16 alpha-hydroxypregnenolone in newborn infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
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Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroids.通过尿甾体类化合物的气相色谱-质谱联用技术诊断新生儿21-羟化酶缺乏症。
Aust Paediatr J. 1988 Oct;24(5):280-5. doi: 10.1111/j.1440-1754.1988.tb01363.x.
4
The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern.
Clin Chim Acta. 1982 Apr 23;120(3):341-53. doi: 10.1016/0009-8981(82)90375-8.
5
A paradox: elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency.一个悖论：21-羟化酶缺乏的新生儿中21-羟孕烯醇酮生成增加。
Steroids. 1987 Apr-May;49(4-5):295-311. doi: 10.1016/0039-128x(87)90006-7.
6
Congenital adrenal hyperplasia due to deficiency of 11 -hydroxylation of 17 -hydroxylated steroids.由于17-羟化类固醇11-羟化作用缺乏所致的先天性肾上腺皮质增生症。
J Clin Endocrinol Metab. 1971 Sep;33(3):501-8. doi: 10.1210/jcem-33-3-501.
7
Serum 17-hydroxypregnenolone and 17-hydroxypregnenolone sulfate concentrations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Endocrinol Jpn. 1988 Feb;35(1):11-8. doi: 10.1507/endocrj1954.35.11.
8
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by amniotic fluid steroid analysis.
Prenat Diagn. 1982 Apr;2(2):97-102. doi: 10.1002/pd.1970020204.
9
Steroid spectrum in human urine as revealed by gas chromatography V. Identification and quantitation of 3 alpha, 20 alpha-dihydroxy-5-beta pregnan-11-one (11-keto-pregnanediol) during different stages of development in children with C/21 hydroxylase deficiency.气相色谱法揭示的人尿中类固醇谱 V. 21-羟化酶缺乏症儿童不同发育阶段3α,20α-二羟基-5-β-孕烷-11-酮（11-酮孕烷二醇）的鉴定与定量分析
Acta Biochim Biophys Acad Sci Hung. 1981;16(3-4):179-88.
10
New identified 15 beta-hydroxylated 21-deoxy-pregnanes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.在21-羟化酶缺乏所致先天性肾上腺皮质增生症中新鉴定出的15β-羟基化21-脱氧孕烷。
J Steroid Biochem Mol Biol. 1993 May;45(5):421-34. doi: 10.1016/0960-0760(93)90011-k.

引用本文的文献

1
Steroid Metabolome Analysis in Disorders of Adrenal Steroid Biosynthesis and Metabolism.肾上腺类固醇生物合成和代谢障碍的类固醇代谢组学分析。
Endocr Rev. 2019 Dec 1;40(6):1605-1625. doi: 10.1210/er.2018-00262.
2
Novel methods in adrenal research: a metabolomics approach.肾上腺研究中的新方法：代谢组学方法。
Histochem Cell Biol. 2019 Mar;151(3):201-216. doi: 10.1007/s00418-019-01772-w. Epub 2019 Feb 6.
3
15 beta-hydroxylated steroids may be diagnostically misleading in confirming congenital adrenal hyperplasia suspected by a newborn screening programme.
15β-羟基化类固醇在通过新生儿筛查项目怀疑先天性肾上腺皮质增生症的确诊中可能具有诊断误导性。
Eur J Pediatr. 1996 Nov;155(11):928-31. doi: 10.1007/BF02282880.
4
Biochemical aspects of congenital adrenal hyperplasia.
J Inherit Metab Dis. 1986;9 Suppl 1:124-34. doi: 10.1007/BF01800866.
5
Urinary excretion of 17-hydroxypregnanolones in patients with different forms of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
Eur J Pediatr. 1992 Jan;151(1):24-8. doi: 10.1007/BF02073884.