Hydrocortisone Dosing during Puberty in Patients with Classical Congenital Adrenal Hyperplasia: An Evidence-Based Recommendation

Author:

Bonfig Walter1,Dalla Pozza Susanne Bechtold1,Schmidt Heinrich1,Pagel Philipp2,Knorr Dietrich1,Schwarz Hans Peter1

Affiliation:

1. University Children’s Hospital (W.B., S.B.D.P., H.S., D.K., H.P.S.), Ludwig Maximilians University, Division of Pediatric Endocrinology, D-80337 Munich, Germany

2. Division of Bioinformatics (P.P.), Technical University, D-80337 Munich, Germany

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference36 articles.

1. Congenital adrenal hyperplasia.;Speiser;N Engl J Med,2003

2. Congenital adrenal hyperplasia—a continuum of disorders.;Hughes;Lancet,1998

3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.;Cutler Jr;N Engl J Med,1990

4. A preliminary study of flutamide, testolactone, and reduced hydrocortisone dose in the treatment of congenital adrenal hyperplasia.;Laue;J Clin Endocrinol Metab,1996

5. Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.;Einaudi;J Pediatr Endocrinol,1993

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