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

Academic Article

Abstract

  • 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.
  • Authors

    Digital Object Identifier (doi)

    Author List

  • Speiser PW; Azziz R; Baskin LS; Ghizzoni L; Hensle TW; Merke DP; Meyer-Bahlburg HFL; Miller WL; Montori VM; Oberfield SE
  • Start Page

  • 494173
  • Volume

  • 2010