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pro vyhledávání: '"Patrizia Matarazzo"'
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 19, p 5767 (2022)
3beta-hydroxysteroid dehydrogenase type II deficiency (HSD3B2 deficiency), a rare form of congenital adrenal hyperplasia (CAH), is characterized by varying degrees of salt loss and incomplete masculinization in males and mild virilization or normal e
Externí odkaz:
https://doaj.org/article/269a5dfe347a4b37b0599fd74d175823