Nutrition management of congenital glucose–galactose malabsorption
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DOI: 10.1097/md.0000000000016828
Abstract: Abstract 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… read more here.
Keywords: glucose galactose; galactose malabsorption; glucose; nutrition management ... See more keywords
Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review
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DOI: 10.3390/diagnostics13020294
Abstract: 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… read more here.
Keywords: glucose galactose; galactose malabsorption; malabsorption; published studies ... See more keywords