The management of achondroplasia in Italy: results from a Delphi panel based on real-world experience

BACKGROUND: Achondroplasia is a rare genetic disorder caused by a mutation in the FGFR3 gene, leading to skeletal changes and other systemic complications that greatly impact the patient's quality of life. There currently are differences in achondroplasia patients' management among countri...

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Detalles Bibliográficos
Autores principales: Maghnie, Mohamad, Bruzzi, Paolo, Casilli, Giorgio, Lidonnici, Dario, Scarano, Gioacchino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315838/
https://www.ncbi.nlm.nih.gov/pubmed/37404559
http://dx.doi.org/10.3389/fped.2023.1209994

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315838/
https://www.ncbi.nlm.nih.gov/pubmed/37404559
http://dx.doi.org/10.3389/fped.2023.1209994

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