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New Developments in the Treatment of X-Linked Hypophosphataemia: Implications for Clinical Management

X-linked hypophosphataemia (XLH) is due to mutations in phosphate-regulating gene with homologies to endopeptidases on the X chromosome (PHEX) and represents the most common heritable form of rickets. In this condition, the hormone fibroblast growth factor 23 (FGF23) is produced in excessive amounts...

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Detalles Bibliográficos
Autores principales: Saraff, Vrinda, Nadar, Ruchi, Högler, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7083817/
https://www.ncbi.nlm.nih.gov/pubmed/31965544
http://dx.doi.org/10.1007/s40272-020-00381-8