中国第一批罕见病目录释义(手册版)
上QQ阅读APP看书,第一时间看更新

参考文献

[1]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-羟化酶缺陷诊治共识 . 中华儿科杂志,2016,54(8):569-576.

[2]顾学范,周建德,叶军,等.上海地区新生儿先天性肾上腺皮质增生症的筛查 .中华预防医学杂志,2002,36(1):16-18.

[3]Melmed S,Polonsky K,Larsen PR,et al. Williams Textbook of Endocrinology(13th Edition) Hardcover ISBN:9780323297387,eBook ISBN:9780323341578.

[4]Mass Screening Committee; Japanese Society for Pediatric Endocrinology;Japanese Society for Mass Screening,Ishii T,Anzo M,Adachi M,et al.Guidelines for diagnosis and treatment of 21-hydroxylase deficiency(2014 revision).Clin Pediatr Endocrinol,2015,24(3):77-105.

[5]Speiser PW,Azziz R,Baskin LS,et al. Endocrine Society. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency:an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab,2010,95(9):4133-4160.