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

BACKGROUND: Classic 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 rep...

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Detalles Bibliográficos
Autores principales: Auchus, Richard J., Courtillot, Carine, Dobs, Adrian, El-Maouche, Diala, Falhammar, Henrik, Lacroix, Andre, Farrar, Mallory, O’Donoghue, Conor, Anatchkova, Milena, Cutts, Katelyn, Taylor, Natalie, Yonan, Chuck, Lamotte, Mark, Touraine, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9717438/
https://www.ncbi.nlm.nih.gov/pubmed/36465641
http://dx.doi.org/10.3389/fendo.2022.1005963

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9717438/
https://www.ncbi.nlm.nih.gov/pubmed/36465641
http://dx.doi.org/10.3389/fendo.2022.1005963

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