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Article

[Clinical and genetic characteristics of 165 children with salt-wasting 21-hydroxylase deficiency in Henan Province].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 15 Apr 2026

Yang Hai-Hua, Huang Ai, Li Yuan, Chen Yong-Xing, Wei Hai-Yan

Abstract excerpt

OBJECTIVES: To explore the clinical and genetic characteristics of children with salt-wasting (SW) 21-hydroxylase deficiency (21-OHD) in Henan Province. METHODS: Clinical characteristics, laboratory results, and genetic findings were retrospectively reviewed for 165 children with SW 21-OHD who presented to the Department of Endocrinology and Genetic Metabolism, Children's Hospital Affiliated to Zhengzhou...

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Share to Adrenal Hyperplasia, Congenital
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42015704
DOI: 10.7499/j.issn.1008-8830.2506116
PMCID: PMC13108933

Genes

CYP21A2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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