Longitudinal 12-Month Follow-Up of a Male Infant with <i>CYP21A2</i> Compound Heterozygous Genotype in China: A Case Report

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Bibliographic Details
Main Authors:	Yi Yin, Xinyue Huang, Yun Shi, Cheng Huang, Jian Yu, Qingsong Liu
Format:	Article
Language:	English
Published:	Thieme Medical Publishers, Inc. 2025-07-01
Series:	American Journal of Perinatology Reports
Subjects:	21-hydroxylase deficiency hyponatremia and hyperkalemia hyperpigmentation molecular genetic diagnosis infant timely therapeutic intervention follow-up
Online Access:	http://www.thieme-connect.de/DOI/DOI?10.1055/a-2647-4369
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