Most Short Children with Cystic Fibrosis Do Not Catch Up by Adulthood

Poor linear growth is common in children with cystic fibrosis (CF) and predicts pulmonary status and mortality. Growth impairment develops in infancy, prior to pulmonary decline and despite aggressive nutritional measures. We hypothesized that growth restriction during early childhood in CF is assoc...

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Detalles Bibliográficos
Autores principales: Marks, Margaret P., Heltshe, Sonya L., Baines, Arthur, Ramsey, Bonnie W., Hoffman, Lucas R., Stalvey, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703459/
https://www.ncbi.nlm.nih.gov/pubmed/34959966
http://dx.doi.org/10.3390/nu13124414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8703459/
https://www.ncbi.nlm.nih.gov/pubmed/34959966
http://dx.doi.org/10.3390/nu13124414

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