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

BackgroundCongenital 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 deficiency...

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主要な著者:	Agustini Utari, Sultana M. H. Faradz, Annastasia Ediati, Tuula Rinne, Mahayu Dewi Ariani, Achmad Zulfa Juniarto, Stenvert L. S. Drop, Antonius E. van Herwaarden, Hedi L. Claahsen-van der Grinten
フォーマット:	Artigo
言語:	Inglês
出版事項:	Frontiers Media S.A. 2022-12-01
シリーズ:	Frontiers in Endocrinology
主題:	congenital adrenal hyperplasia CYP11B1 deficiency differences (disorders) of sex development developing country guideline
オンライン･アクセス:	https://www.frontiersin.org/articles/10.3389/fendo.2022.1015973/full
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