Current and future perspectives on clinical management of classic 21-hydroxylase deficiency
Author:
Affiliation:
1. Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo 113-8510, Japan
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://www.jstage.jst.go.jp/article/endocrj/70/10/70_EJ23-0075/_pdf
Reference91 articles.
1. 1 Speiser PW, White PC (2003) Congenital adrenal hyperplasia. N Engl J Med 349: 776–788.
2. 2 Claahsen-van der Grinten HL, Speiser PW, Ahmed SF, Arlt W, Auchus RJ, et al. (2022) Congenital adrenal hyperplasia-current insights in pathophysiology, diagnostics, and management. Endocr Rev 43: 91–159.
3. 3 White PC, New MI, Dupont B (1987) Congenital adrenal hyperplasia. (1). N Engl J Med 316: 1519–1524.
4. 4 Tsuji A, Konishi K, Hasegawa S, Anazawa A, Onishi T, et al. (2015) Newborn screening for congenital adrenal hyperplasia in Tokyo, Japan from 1989 to 2013: a retrospective population-based study. BMC Pediatr 15: 209.
5. 5 White PC, Speiser PW (2000) Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev 21: 245–291.
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