Send to

Choose Destination
Int J Pediatr Endocrinol. 2010;2010:494173. doi: 10.1155/2010/494173. Epub 2010 Jun 30.

A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency.

Author information

Division of Pediatric Endocrinology, Cohen Children's Medical Center of New York, Hofstra University School of Medicine, 400 Lakeville Rd., Suite 180, New Hyde Park, NY 11040, USA.


Steroid 21-hydroxylase deficiency accounts for about 95% of cases of congenital adrenal hyperplasia (CAH). Newborns are currently being screened for the classical forms of this disease throughout the United States and in 12 other countries. As such, it seems important to develop the best practice guidelines for treating not only infants and children, but affected adults as well. This report gives a brief overview of the most recent expert opinion and clinical practice guidelines for CAH as formulated by The Endocrine Society Task Force.

Supplemental Content

Full text links

Icon for BioMed Central Icon for PubMed Central
Loading ...
Support Center