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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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| Publicado no: | Nat Med |
|---|---|
| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7018602/ https://ncbi.nlm.nih.gov/pubmed/31959989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41591-019-0714-x |
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