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Nutrition management of congenital glucose–galactose malabsorption: Case report of a Chinese infant
RATIONALE: Congenital glucose–galactose malabsorption (CGGM) is a rare, autosomal recessive, hereditary disease that usuallypresents in newborns. CGGM manifests as severe diarrhea, hyperosmolar dehydration, and malnutrition. It does not respond to routine treatment and often is life-threatening. PAT...
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| Pubblicato in: | Medicine (Baltimore) |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wolters Kluwer Health
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6831416/ https://ncbi.nlm.nih.gov/pubmed/31415402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000016828 |
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