Challenges in treatment of patients with non-classic congenital adrenal hyperplasia

Congenital adrenal hyperplasia (CAH) due to 21α-hydroxylase deficiency (21OHD) or 11β-hydroxylase deficiency (11OHD) are congenital conditions with affected adrenal steroidogenesis. Patients with classic 21OHD and 11OHD have a (nearly) complete enzyme deficiency resulting in impaired cortisol synthe...

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Detalles Bibliográficos
Autores principales: Adriaansen, Bas P. H., Schröder, Mariska A. M., Span, Paul N., Sweep, Fred C. G. J., van Herwaarden, Antonius E., Claahsen-van der Grinten, Hedi L.
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/PMC9791115/
https://www.ncbi.nlm.nih.gov/pubmed/36578966
http://dx.doi.org/10.3389/fendo.2022.1064024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791115/
https://www.ncbi.nlm.nih.gov/pubmed/36578966
http://dx.doi.org/10.3389/fendo.2022.1064024

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