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Article

Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.

World journal of pediatrics : WJP - 1 Apr 2024

Lu Wen-Li, Ma Xiao-Yu, Zhang Jiao, Wang Jun-Qi, Zhang Ting-Ting, Ye Lei, Xiao Yuan, Dong Zhi-Ya, Wang Wei, Sun Shou-Yue, Li Chuan-Yin, Hu Rong-Gui, Ning Guang, Zhang Li-Dan

Abstract excerpt

BACKGROUND: The clinical manifestations of nonclassical 11beta-hydroxylase deficiency are very similar to those of non-classical 21-hydroxylase deficiency. For this study, we investigated the relationship between the clinical and molecular features of congenital adrenal hyperplasia caused by 11beta-hydroxylase deficiency and reviewed the related literature, which are expected to provide assistance for the...

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Source

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Identifiers

PMID: 37486441
DOI: 10.1007/s12519-023-00739-1
PMCID: PMC11052800

Genes

CYP11B1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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