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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| 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 |