FGF23 and its role in X-linked hypophosphatemia-related morbidity

FGF23 and its role in X-linked hypophosphatemia-related morbidity

Abstract Background X-linked hypophosphatemia (XLH) is an inherited disease of phosphate metabolism in which inactivating mutations of the Phosphate Regulating Endopeptidase Homolog, X-Linked (PHEX) gene lead to local and systemic effects including impaired growth, rickets, osteomalacia, bone abnorm...

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Bibliographic Details
Main Authors: Signe Sparre Beck-Nielsen, Zulf Mughal, Dieter Haffner, Ola Nilsson, Elena Levtchenko, Gema Ariceta, Carmen de Lucas Collantes, Dirk Schnabel, Ravi Jandhyala, Outi Mäkitie
Format: Article
Language:English
Published: BMC 2019-02-01
Series:Orphanet Journal of Rare Diseases
Subjects:
X-linked hypophosphatemia (XLH)
fibroblast growth factor 23 (FGF23)
phosphate regulating endopeptidase homolog, X-linked (PHEX)
hypophosphatemia
vitamin D deficiency
rickets
Online Access:http://link.springer.com/article/10.1186/s13023-019-1014-8

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http://link.springer.com/article/10.1186/s13023-019-1014-8

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