[1]刘晓琳,高天舒.一例误诊为PCOS的非经典型21-羟化酶缺陷症病例报道[J].国际内分泌代谢杂志,2020,40(06):430-432.[doi:10.3760/cma.j.cn121383-20201223-12068]
　Liu Xiaolin,Gao Tianshu.A case report of atypical 21-hydroxylase deficiency misdiagnosed as PCOS[J].International Journal of Endocrinology and Metabolism,2020,40(06):430-432.[doi:10.3760/cma.j.cn121383-20201223-12068]
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一例误诊为PCOS的非经典型21-羟化酶缺陷症病例报道()
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《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
40
期数:
2020年06期
页码:
430-432
栏目:
病例报告
出版日期:
2020-11-20

文章信息/Info

Title:
A case report of atypical 21-hydroxylase deficiency misdiagnosed as PCOS
作者:
刘晓琳; 高天舒
辽宁中医药大学附属医院内分泌科,沈阳 100032
Author(s):
Liu Xiaolin;  Gao Tianshu
Department of Endocrinology, Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang 110031, China
DOI:
10.3760/cma.j.cn121383-20201223-12068
文献标志码:
A

参考文献/References:

[1] Speiser PW, Arlt W, Auchus RJ, et al.Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency:an Endocrine Society clinical practice guideline[J].J Clin Endocrinol Metab,2018,103(11):1-46.DOI:10.1210/jc.2018-01865.
[2] Mass Screening Committee,Japanese Society for Pediatric Endocrinology,Japanese Society for Mass Screening, et al.Guidelines for diagnosis and treatment of 21-hydroxylase deficiency(2014 revision)[J].Clin Pediatr Endocrinol,2015,24(3):77-105.DOI:10.1297/cpe.24.77.
[3] 中华医学会儿科学分会内分泌遗传代谢病学组. 先天性肾上腺皮质增生症21-羟化酶缺陷诊治指南[J].中国儿科杂志, 2016, 54(8): 569-576.DOI:10.3760/cma.j.issn.0578-1310.2016.08.003.
[4] De Crecchio L. A case report of masculine appearance in a woman[J].Morgagni,1865,7:154-188.
[5] 陆召麟,卢琳.先天性肾上腺皮质增生症:非经典型21羟化酶缺陷症的研究进展[J].内科急危重症杂志,2010,16(1):1-3.
[6] Jayle MF,Weinmann SH,Baulieu EE,et al. Virilisme post-pubertaire discret par deficience de l'hydroxylation enC21[J].Eur J Endocrinol,1958,29(4):513-524.DOI:10.1530/acta.0.0290513.

备注/Memo

备注/Memo:
通信作者:高天舒,Email:gaotianshu67@163.com
更新日期/Last Update: 2020-11-20