The importance of elevated basal 17-hydroxyprogesterone in the diagnosis of children with congenital adrenal hyperplasia

Background: Congenital adrenal hyperplasia (CAH) is usually characterised by a deficiency of 21a-hydroxylase, which causes a deficiency of cortisol and aldosterone and an overproduction of 17-hydroxyprogesterone. The classic and non-classical forms of the disease present ambiguous genitalia with sig...

Ausführliche Beschreibung

Bibliografische Detailangaben

Hauptverfasser:	Miolski Jelena, Ješić Maja, Skakić Anita, Pavlović Sonja, Vorgučin Ivana, Bojić Vladislav, Kovačević Smiljka, Blagojević Jelena, Didić Nevena, Doknić Mirjana, Zdravković Vera
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Society of Medical Biochemists of Serbia, Belgrade 2026-01-01
Schriftenreihe:	Journal of Medical Biochemistry
Schlagworte:	17-hydroxyprogesterone congenital adrenal hyperplasia precocious puberty cyp21a2 heterozygous cyp21a2 gene
Online-Zugang:	https://scindeks-clanci.ceon.rs/data/pdf/1452-8258/2026/1452-82582603566M.pdf
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