PSAT082 A Survey of Patients Living with CAH Assessing Their Perceptions on Glucocorticoid Regimen and Glucocorticoid-Associated Side Effects

BACKGROUND: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) is an autosomal recessive disorder characterized by insufficient cortisol production resulting in excess adrenal androgen production. The standard of care to replace the insufficient cortisol production is the...

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Detalles Bibliográficos
Autores principales: Barnes, Chris, Dias, Rosh, Feather, Melodie, Sherpa-Pine, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624596/
http://dx.doi.org/10.1210/jendso/bvac150.233

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624596/
http://dx.doi.org/10.1210/jendso/bvac150.233

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