X-linked hypophosphatemic rickets: an Italian experts’ opinion survey

BACKGROUND: X-linked hypophosphatemic rickets (XLH) is the first cause of inherited hypophosphatemia and is caused by mutation in the PHEX gene, resulting in excessive expression of the phosphaturic factor FGF23. Symptoms are mainly related to rickets in children and osteomalacia in adults and cause...

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Detalles Bibliográficos
Autores principales: Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., de Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D’Ausilio, A., Lanati, E. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545008/
https://www.ncbi.nlm.nih.gov/pubmed/31151476
http://dx.doi.org/10.1186/s13052-019-0654-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545008/
https://www.ncbi.nlm.nih.gov/pubmed/31151476
http://dx.doi.org/10.1186/s13052-019-0654-6

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