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Infants with cystic fibrosis have altered fecal functional capacities with potential clinical and metabolic consequences
BACKGROUND: Infants with cystic fibrosis (CF) suffer from gastrointestinal (GI) complications, including pancreatic insufficiency and intestinal inflammation, which have been associated with impaired nutrition and growth. Recent evidence identified altered fecal microbiota taxonomic compositions in...
Autores principales: | Eng, Alexander, Hayden, Hillary S., Pope, Christopher E., Brittnacher, Mitchell J., Vo, Anh T., Weiss, Eli J., Hager, Kyle R., Leung, Daniel H., Heltshe, Sonya L., Raftery, Daniel, Miller, Samuel I., Hoffman, Lucas R., Borenstein, Elhanan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444586/ https://www.ncbi.nlm.nih.gov/pubmed/34525965 http://dx.doi.org/10.1186/s12866-021-02305-z |
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