Late consequences of classic congenital adrenal hyperplasia and its long-term poor control in men (case report and literature review)

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...

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Bibliographic Details
Main Authors: Boris M. Shifman, Larisa K. Dzeranova, Ekaterina A. Pigarova, Anatoly N. Tiulpakov, Natalia S. Fedorova
Format: Article
Language:English
Published: Endocrinology Research Centre 2019-12-01
Series:Ожирение и метаболизм
Subjects:
сase reports
adrenal hyperplasia
congenital, 21-hydroxylase deficiency
adult
male
hypercorticism
glucocorticoids
metabolic profile
bmi
obesity
body height
cardiovascular risk
testicular neoplasms
adrenal neoplasms
myelolipoma
osteopenia
Online Access:https://www.omet-endojournals.ru/jour/article/view/10032

Internet

https://www.omet-endojournals.ru/jour/article/view/10032

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