Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review

Glucose-galactose malabsorption is a rare inherited autosomal recessive genetic defect. A mutation in the glucose sodium-dependent transporter-1 gene will alter the transportation and absorption of glucose and galactose in the intestine. The defect in the SGLT-1 leads to unabsorbed galactose, glucos...

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Detalles Bibliográficos
Autores principales: Alruwaili, Nawaf W., Alshdayed, Fahad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857642/
https://www.ncbi.nlm.nih.gov/pubmed/36673104
http://dx.doi.org/10.3390/diagnostics13020294

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9857642/
https://www.ncbi.nlm.nih.gov/pubmed/36673104
http://dx.doi.org/10.3390/diagnostics13020294

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