Treatment patterns and unmet needs in adults with classic congenital adrenal hyperplasia: A modified Delphi consensus study

BackgroundClassic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is a rare autosomal recessive condition characterized by cortisol deficiency and excess androgen production. The current standard of care is glucocorticoid (GC) therapy, and sometimes mineralocorticoids, to repla...

Full description

Bibliographic Details
Main Authors: Richard J. Auchus, Carine Courtillot, Adrian Dobs, Diala El-Maouche, Henrik Falhammar, Andre Lacroix, Mallory Farrar, Conor O’Donoghue, Milena Anatchkova, Katelyn Cutts, Natalie Taylor, Chuck Yonan, Mark Lamotte, Philippe Touraine
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.1005963/full