What to Expect of Feeding Abilities and Nutritional Aspects in Achondroplasia Patients: A Narrative Review

Achondroplasia is an autosomal dominant genetic disease representing the most common form of human skeletal dysplasia: almost all individuals with achondroplasia have identifiable mutations in the fibroblast growth factor receptor type 3 (FGFR3) gene. The cardinal features of this condition and its...

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Detalles Bibliográficos
Autores principales: Sforza, Elisabetta, Margiotta, Gaia, Giorgio, Valentina, Limongelli, Domenico, Proli, Francesco, Kuczynska, Eliza Maria, Leoni, Chiara, De Rose, Cristina, Trevisan, Valentina, Romeo, Domenico Marco, Calandrelli, Rosalinda, De Corso, Eugenio, Massimi, Luca, Palmacci, Osvaldo, Rigante, Donato, Zampino, Giuseppe, Onesimo, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858955/
https://www.ncbi.nlm.nih.gov/pubmed/36672940
http://dx.doi.org/10.3390/genes14010199

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