Challenges in the treatment of late-identified untreated congenital adrenal hyperplasia due to CYP11B1 deficiency: Lessons from a developing country

BACKGROUND: Congenital Adrenal Hyperplasia (CAH) due to CYP11B1 is a rare autosomal recessive adrenal disorder that causes a decrease in cortisol production and accumulation of adrenal androgens and steroid precursors with mineralocorticoid activity. Clinical manifestations include cortisol deficien...

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Detalles Bibliográficos
Autores principales: Utari, Agustini, Faradz, Sultana M. H., Ediati, Annastasia, Rinne, Tuula, Ariani, Mahayu Dewi, Juniarto, Achmad Zulfa, Drop, Stenvert L. S., 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/PMC9797803/
https://www.ncbi.nlm.nih.gov/pubmed/36589846
http://dx.doi.org/10.3389/fendo.2022.1015973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797803/
https://www.ncbi.nlm.nih.gov/pubmed/36589846
http://dx.doi.org/10.3389/fendo.2022.1015973

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