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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Detalles Bibliográficos
Autores principales: Ma, Ming, Long, Qi, Chen, Fei, Zhang, Ting, Lu, Mengshan, Wang, Weiyan, Chen, Lihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
5500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831416/
https://www.ncbi.nlm.nih.gov/pubmed/31415402
http://dx.doi.org/10.1097/MD.0000000000016828

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831416/
https://www.ncbi.nlm.nih.gov/pubmed/31415402
http://dx.doi.org/10.1097/MD.0000000000016828

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