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Article

[Genetic and clinical analysis of X-linked hypophosphatemic rickets].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Aug 2021

Wei L Y, Gong C X, Cao B Y, Li X Q, Liang X J, Li W J, Wu D, Liu M, Su C, Chen J J

Abstract excerpt

Objective: To investigate the clinical and genetic features, and treatment of X-linked hypophosphatemic rickets (XLH). Methods: In this retrospective study, we reviewed the medical records of 25 pediatric patients with XLH who were admitted to Department of Endocrinology Genetics and Metabolism,Beijing Children's Hospital from January 2010 to January 2020. The clinical characteristics, PHEX gene variants, as well...

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Identifiers

PMID: 34333921
DOI: 10.3760/cma.j.cn112140-20210311-00201

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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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