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X-linked hypophosphatemic rickets and nephrocalcinosis: clinical characteristics of a single-center pediatric cohort in North America before and after burosumab

BackgroundX-linked hypophosphatemic rickets (XLH) is a rare genetic disease characterized by inappropriately elevated circulating fibroblast growth factor 23 (FGF-23) and subsequent urinary phosphate wasting. The primary clinical manifestations of XLH include short stature, lower extremity bowing, d...

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Bibliografische Detailangaben
Hauptverfasser: Neil J. Paloian, Lindsey R. Boyke-Lohmann, Robert D. Steiner
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2024-08-01
Schriftenreihe:Frontiers in Pediatrics
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Online-Zugang:https://www.frontiersin.org/articles/10.3389/fped.2024.1430921/full
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