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Partial 3 -hydroxysteroid dehydrogenase (3 -HSD) deficiency in a family with congenital adrenal hyperplasia: evidence for increasing 3 -HSD activity with age.

作者信息

Kenny F M, Reynolds J W, Green O C

出版信息

Pediatrics. 1971 Nov;48(5):756-65.

PMID:4256344
Abstract
摘要

相似文献

1
Partial 3 -hydroxysteroid dehydrogenase (3 -HSD) deficiency in a family with congenital adrenal hyperplasia: evidence for increasing 3 -HSD activity with age.
Pediatrics. 1971 Nov;48(5):756-65.
2
Gas-liquid chromatographic fractionation of the urinary 17-oxo- and 17-oxogenic steroids; a simple qualitative aid in the diagnosis and treatment of adrenocortical dysfunction.
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[Adrenal hirsutism (3-beta-hydroxysteroid dehydrogenase deficiency). Studies using chromatographic separation of the urinary 17-ketosteroid fraction. 3. On the differential diagnosis of adrenal hirsutism (M. Cushing, congenital adrenogenital syndrome)].[肾上腺性多毛症（3-β-羟类固醇脱氢酶缺乏症）。利用尿17-酮类固醇组分色谱分离的研究。3. 关于肾上腺性多毛症的鉴别诊断（库欣综合征、先天性肾上腺皮质增生症）]
Endokrinologie. 1968 Feb;52(5):289-314.
4
[Influence of dehydroepiandrosterone on the secretion of corticoids].
Endokrinologie. 1964;46(5):298-301.
5
The identification of C19-16-unsaturated steroids and estimation of 17-oxosteroids in boar spermativ vein plasma and urine.公猪精液静脉血浆和尿液中C19 - 16 - 不饱和类固醇的鉴定及17 - 氧类固醇的测定。
J Endocrinol. 1970 Jul;47(3):357-65.
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
Studies of androgens and their precursors in adrenocortical virilizing carcinoma.肾上腺皮质男性化癌中雄激素及其前体的研究。
J Clin Endocrinol Metab. 1971 Apr;32(4):462-9. doi: 10.1210/jcem-32-4-462.
8
An unusual form of adrenogenital syndrome.一种不寻常形式的肾上腺生殖器综合征。
Endokrinologie. 1971 Apr;57(3):343-7.
9
Malignant lipid cell tumor of the ovary: clinical, biochemical and etiologic considerations.卵巢恶性脂质细胞瘤：临床、生化及病因学考量
J Clin Endocrinol Metab. 1970 Mar;30(3):336-44. doi: 10.1210/jcem-30-3-336.
10
Plasma and urinary steroids in an eight-year-old boy with 3-beta-hydxysteroid dehydrogenase deficiency.
J Clin Endocrinol Metab. 1970 Aug;31(2):162-5. doi: 10.1210/jcem-31-2-162.

引用本文的文献

1
Human 3beta-hydroxysteroid dehydrogenase deficiency associated with normal spermatic numeration despite a severe enzyme deficit.尽管存在严重的酶缺乏，但人类3β-羟基类固醇脱氢酶缺乏症与正常精子计数相关。
Endocr Connect. 2018 Mar;7(3):395-402. doi: 10.1530/EC-17-0306. Epub 2018 Feb 2.
2
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency.3β-羟基类固醇脱氢酶缺乏所致先天性肾上腺皮质增生症
Eur J Pediatr. 1996 Apr;155(4):259-61. doi: 10.1007/BF02002710.
3
Urinary excretion delta 5-pregnenetriol (5-pregnene-3 beta, 17 alpha, 20-triol) in healthy children.
Eur J Pediatr. 1980 Aug;134(2):103-7. doi: 10.1007/BF01846025.
4
Steroid enzyme defects leading to male pseudohermaphroditism.导致男性假两性畸形的类固醇酶缺陷。
Indian J Pediatr. 1992 Jul-Aug;59(4):501-14. doi: 10.1007/BF02751568.
5
Male hypogonadism.男性性腺功能减退
West J Med. 1976 Jun;124(6):446-75.
6
Male pseudohermaphroditism: genetics and clinical delineation.男性假两性畸形：遗传学与临床描述
Hum Genet. 1978 Oct 19;44(1):1-49. doi: 10.1007/BF00283573.
7
Persistent testicular delta5-isomerase-3beta-hydroxysteroid dehydrogenase (delta5-3beta-HSD) deficiency in the delta5-3beta-HSD form of congenital adrenal hyperplasia.先天性肾上腺皮质增生症δ5-3β-羟类固醇脱氢酶（δ5-3β-HSD）型中的持续性睾丸δ5-异构酶-3β-羟类固醇脱氢酶（δ5-3β-HSD）缺乏症
J Clin Invest. 1975 Apr;55(4):681-90. doi: 10.1172/JCI107977.