Late consequences of classic congenital adrenal hyperplasia and its long-term poor control in men (case report and literature review)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) is an autosomal recessive disorder of the adrenal cortex characterized by impairment of cortisol biosynthesis (with possible impairment of aldosterone biosynthesis) and excessive pituitary ACTH release, which promotes ove...
| 出版年: | Ожирение и метаболизм |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Endocrinology Research Centre
2019-12-01
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| 主題: | |
| オンライン･アクセス: | https://www.omet-endojournals.ru/jour/article/view/10032 |