Auxological and Endocrinological Features in Children and Adolescents with Cystic Fibrosis

Cystic fibrosis (CF) is a multisystem autosomal recessive disease caused by mutations that lead to deficient or dysfunctional CF transmembrane conductance regulator (CFTR) proteins. Patients typically present malnutrition resulting from the malabsorption of fundamental nutrients and recurring lung i...

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Detalles Bibliográficos
Autores principales: Ferrari, Vittorio, Terlizzi, Vito, Stagi, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323690/
https://www.ncbi.nlm.nih.gov/pubmed/35887806
http://dx.doi.org/10.3390/jcm11144041

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323690/
https://www.ncbi.nlm.nih.gov/pubmed/35887806
http://dx.doi.org/10.3390/jcm11144041

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