Congenital Adrenal Hyperplasia

Author:

Speiser Phyllis W.

Abstract

Congenital adrenal hyperplasia associated with deficiency of steroid 21-hydroxylase is the most common inborn error in adrenal function and the most common cause of adrenal insufficiency in the pediatric age group. As patients now survive into adulthood, adult health-care providers must also be familiar with this condition. Over the past several years, F1000 has published numerous commentaries updating research and practical guidelines for this condition. The purposes of this review are to summarize basic information defining congenital adrenal hyperplasia and to highlight current knowledge and controversies in management.

Publisher

F1000 Research Ltd

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference24 articles.

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4. One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study.;S Gidlöf;Lancet Diabetes Endocrinol.,2013

5. Neonatal screening for congenital adrenal hyperplasia in Japan.;T Tajima;Pediatr Endocrinol Rev.,2012

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