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Burosumab in infants with X-linked hypophosphatemic rickets: a case series

Abstract Background X-linked hypophosphatemic rickets (XLH) is a rare inherited metabolic bone disorder caused by excess fibroblast growth factor 23 (FGF23), leading to hypophosphatemia and rickets. Burosumab, a human monoclonal antibody targeting FGF23, was approved for the treatment of XLH in Apri...

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Hlavní autoři: Ravit Regev, Avivit Brener, Nitzan Dror, Raphael Krespi, Rebeca Rapalino, Efrat Chorna, Ophir Borger, Adar Lopez, Yael Lebenthal, Leonid Zeitlin
Médium: Artigo
Jazyk:Inglês
Vydáno: BMC 2026-01-01
Edice:Orphanet Journal of Rare Diseases
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On-line přístup:https://doi.org/10.1186/s13023-025-04177-2
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