Fecal dysbiosis in infants with cystic fibrosis is associated with early linear growth failure

Most infants with cystic fibrosis (CF) have pancreatic exocrine insufficiency that results in nutrient malabsorption and requires oral pancreatic enzyme replacement. Newborn screening for CF has enabled earlier diagnosis, nutritional intervention, and enzyme replacement for these infants, allowing m...

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Detalles Bibliográficos
Autores principales: Hayden, HS, Eng, A, Pope, CE, Brittnacher, MJ, Vo, AT, Weiss, EJ, Hager, KR, Martin, BD, Leung, DH, Heltshe, SL, Borenstein, E, Miller, SI, Hoffman, LR
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018602/
https://www.ncbi.nlm.nih.gov/pubmed/31959989
http://dx.doi.org/10.1038/s41591-019-0714-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018602/
https://www.ncbi.nlm.nih.gov/pubmed/31959989
http://dx.doi.org/10.1038/s41591-019-0714-x

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