PSAT095 Examination of Treatment Patterns in Patients with Classic Congenital Adrenal Hyperplasia (CAH) Compared to Treatment Guidelines

INTRODUCTION: Classic congenital adrenal hyperplasia (CAH) is a rare autosomal recessive disorder, usually due to a deficiency in the 21-hydroxylase enzyme, that results in impaired cortisol synthesis and excess androgen production. Recommended guidelines for management of CAH include assessment of...

Descripción completa

Detalles Bibliográficos
Autores principales: Manahan, Rachel, Farrar, Mallory, O’Donoghue, Conor, Paiewonsky, Ed, Yonan, Chuck, Nathan, Ramaa, Pfeffer, Daniel, Tiwari, Vinayak, Shripathi, Prasad, Russo, Pierantonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624727/
http://dx.doi.org/10.1210/jendso/bvac150.238

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624727/
http://dx.doi.org/10.1210/jendso/bvac150.238

Ejemplares similares