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非经典型21-羟化酶缺陷症的诊治 被引量:6

Diagnosis and treatment for nonclassic 21-hydroxylase deficiency
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作者 宁光 杨军
出处 《中国实用内科杂志》 CAS CSCD 北大核心 2007年第23期1816-1818,共3页 Chinese Journal of Practical Internal Medicine
关键词 先天性肾上腺增生症 21-羟化酶缺陷症 非经典型 17-羟孕酮 Congenital adrenal hyperplasia 21-Hydroxylase deficiency, nonclassic 17-Hydroxyprogesterone
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  • 2Jayle MF,Weinmann SH, Baulieu EE,et al. Virilisme post-pubertaire discret par deficience de l'hydroxylation enC21 [ J ]. Acta Endocrinol( Copenh ), 1958,29:513-524. 被引量:1
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  • 7Weintrob N, Brautbar C, Pertzelan A, et al. Genotype-phenotype associations in non-classical steroid 21 hydroxylase deficiency[J]. Eur J Endoerinol,2000,143 :397-403. 被引量:1
  • 8Tajima T, Fujieda K,Nakae J, et al. Mutations of the CYP21 gene in nonclassical steroid 21 hydroxylase deficiency in Japan[ J ]. Endocr J, 1998,45:493-497. 被引量:1
  • 9Rogerio S, Araujo, Ana EC,et al. Substitutions in the CYP21A2 promoter explain the simple virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation [ J ]. Clin Endocrinol,2005,62 : 132-136. 被引量:1
  • 10Romaguera J, Moran C, Diaz-Montes TP, et al. Prevalence of 21hydroxylase-deficient nonclassic adrenal hyperplasia and insulin resistance among hirsute women from Puerto Rico[ J ]. Fertil Steril,2000,74:59-62. 被引量:1

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