Interpretation of Steroid Biomarkers in 21-Hydroxylase Deficiency and Their Use in Disease Management

The most common form of congenital adrenal hyperplasia is 21-hydroxylase deficiency (21OHD), which in the classic (severe) form occurs in roughly 1:16 000 newborns worldwide. Lifelong treatment consists of replacing cortisol and aldosterone deficiencies, and supraphysiological dosing schedules are t...

Descripción completa

Detalles Bibliográficos
Autores principales: Sarafoglou, Kyriakie, Merke, Deborah P, Reisch, Nicole, Claahsen-van der Grinten, Hedi, Falhammar, Henrik, Auchus, Richard J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Mini-Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438890/
https://www.ncbi.nlm.nih.gov/pubmed/36950738
http://dx.doi.org/10.1210/clinem/dgad134

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10438890/
https://www.ncbi.nlm.nih.gov/pubmed/36950738
http://dx.doi.org/10.1210/clinem/dgad134

Ejemplares similares