Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood
Author:
Affiliation:
1. Department of Human Ontogeny and Childhood Development, Tokyo Medical and Dental University
2. Division of Pediatrics and Child Neurology, Department of Brain and Nerve Science, Oita University
Publisher
Japan Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://www.jstage.jst.go.jp/article/endocrj/55/2/55_K07E-057/_pdf
Reference20 articles.
1. 1. New MI (2006) Extensive clinical experience: nonclassical (2006) 21-hydroxylase deficiency. J Clin Endocrinol Metab 11: 4205-4214.
2. 2. Newfield RS, New MI (1997) 21-hydroxylase deficiency. Ann N Y Acad Sci 17: 219-229.
3. Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
4. 4. White PC, New MI, Dupont B (1987) Congenital Adrenal Hyperplasia. N Engl J Med 316: 1519-1524.
5. Congenital Adrenal Hyperplasia
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