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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Detalhes bibliográficos
Publicado no:Front Endocrinol (Lausanne)
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Endocrinology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8018222/
https://ncbi.nlm.nih.gov/pubmed/33815285
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2021.626646
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