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SUN-523 XLH Outcome Data from One Centre Experience with Burosumab

X-linked hypophosphataemia (XLH) is a rare, genetic, chronically debilitating and deformative bone disease that profoundly impacts the affected individual’s day-to-day functioning and quality of life. High levels of circulating fibroblast growth factor 23 (FGF23) lead to excess urinary phosphate exc...

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Detalles Bibliográficos
Autores principales: Cheung, Moira, Sakka, Sophia, Gilbey-Cross, Robyn, Harries, Mark, Mathieson, Leigh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6553073/
http://dx.doi.org/10.1210/js.2019-SUN-523