Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) is a disorder of adrenal steroid biosynthesis, leading to hypocortisolism, hypoaldosteronism, and hyperandrogenism. Impaired quality of life (QoL) has been demonstrated in women with CAH, but data on men with CAH are scarc...

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Detalles Bibliográficos
Autores principales: Verhees, Myrthe J. M., Engels, Manon, Span, Paul N., Sweep, Fred C. G. J., van Herwaarden, Antonius E., Falhammar, Henrik, Nordenström, Anna, Webb, Emma A., Richter-Unruh, Annette, Bouvattier, Claire, de la Perrière, Aude Brac, Arlt, Wiebke, Reisch, Nicole, Köhler, Birgit, Rapp, Marion, Stikkelbroeck, Nike M. M. L., Roeleveld, Nel, Claahsen-van der Grinten, Hedi L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018222/
https://www.ncbi.nlm.nih.gov/pubmed/33815285
http://dx.doi.org/10.3389/fendo.2021.626646

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8018222/
https://www.ncbi.nlm.nih.gov/pubmed/33815285
http://dx.doi.org/10.3389/fendo.2021.626646

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