Naslov
Untreated congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Autori
Tahirović, Husref ; Toromanović, Alma ; Grubi, Marina ; Grubić, Zorana ; Dumić, Katja

Izvornik
European journal of pediatrics (0340-6199) 168 (2009), 7; 847-849

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
congenital adrenal hyperplasia ; untreated

Sažetak
Congenital adrenal hyperplasia (CAH) is an inherited metabolic disease caused by the deficiency of one of the enzymes necessary for cortisol synthesis. With carefully supervised medical treatment, CAH patients have the capacity for normal puberty and fertility. We report on a 12.4-year-old female who, because of the early interruption of treatment, developed progressive virilization with reduced final height and altered psycho-social orientation to male. One of the reasons for interrupting replacement therapy in our case was the difficult social and economic status of the family, who lived for many years without basic medical care.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti

POVEZANOST RADA