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Article

Nonclassic 21-hydroxylase deficiency in Croatia.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Feb 2004

Dumic Miroslav, Ille Jasenka, Zunec Renata, Plavsic Vesna, Francetic Igor, Skrabic Veselin, Janjanin Nevena, Spehar Anita, Wei JiQing, Wilson Robert C, New Maria I

Abstract excerpt

This is the first report of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase (21-OH) deficiency in Croatia in which the patients have been evaluated clinically, hormonally, and by molecular genetic analysis. Genetic analysis was performed on 18 Croatian patients with nonclassic CAH due to 21-OH deficiency using allele-specific PCR. ACTH stimulation testing and HLA typing were used to evaluate...

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Share to 17-alpha-Hydroxyprogesterone
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15055349
DOI: 10.1515/jpem.2004.17.2.157

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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