Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia

Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia

ObjectiveThe aim of this study was to fully describe the clinical and genetic characteristics, including clinical manifestations, intact fibroblast growth factor 23 (iFGF23) levels, and presence of PHEX gene mutations, of 22 and 7 patients with familial and sporadic X-linked dominant hypophosphatemi...

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Bibliographic Details
Main Authors: Tian Xu, Xiaohui Tao, Zhenlin Zhang, Hua Yue
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-08-01
Series:Frontiers in Endocrinology
Subjects:
X-linked dominant hypophosphatemia
PHEX
fibroblast growth factor 23
clinical features
gene mutation
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2022.956646/full

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https://www.frontiersin.org/articles/10.3389/fendo.2022.956646/full

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