Neurofibromatosis type I (NF1) and bone involvement in a pediatric setting: insights from FGF23 levels

Abstract Background Neurofibromatosis type I (NF1) is an autosomal dominant disorder characterized by extremely different phenotypes, sometimes including reduced bone mass. The underlying cause of bone impairment in these patients remains poorly understood, especially in children. Previous studies i...

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Autors principals:	Giulia Rodari, Valeria Citterio, Masami Ikehata, Deborah Mattinzoli, Giulietta Scuvera, Federico Grilli, Eriselda Profka, Federico Giacchetti, Valentina Collini, Alessandro Risio, Claudia Cesaretti, Federica Natacci, Carlo Alfieri, Giovanna Mantovani, Claudia Giavoli
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2025-03-01
Col·lecció:	Italian Journal of Pediatrics
Matèries:	Neurofibromatosis type I NF1 FGF23 Bone
Accés en línia:	https://doi.org/10.1186/s13052-025-01941-9
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