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Glucose Galactose Malabsorption

Congenital glucose-galactose malabsorption
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Glucose Galactose Malabsorption" returned 0 free, full-text review articles. First 0 results:
Molecular basis for glucose-galactose malabsorption.
Last Updated: Nov 21, 2013

Glucose-galactose malabsorption (GGM) is an autosomal recessive disease that presents in newborn infants as a life-threatening diarrhea. The diarrhea ceases within 1 h of removing oral intake of lactose, glucose, and galactose, but promptly returns with the introduction of one or ...

I. Glucose galactose malabsorption.
Last Updated: Feb 26, 2019

Glucose Galactose Malabsorption is a genetic disorder caused by a defect in glucose and galactose transport across the intestinal brush border. Normally, lactose in milk is broken down into glucose and galactose by lactase, an ectoenzyme on the brush border, and the hexoses are transported ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Glucose Galactose Malabsorption" returned 0 free, full-text editorial articles. First 0 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Glucose Galactose Malabsorption" returned 10 free, full-text research articles. First few results:
Nutrition management of congenital glucose-galactose malabsorption: Case report of a Chinese infant.
Last Updated: Nov 20, 2019

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.

SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption.
Last Updated: Apr 15, 2019

Congenital glucose-galactose malabsorption (cGGM) is a rare autosomal recessive disorder, caused by mutations in the SLC5A1 gene, encoding the sodium/glucose cotransporter 1, which may result in severe life-threatening osmotic diarrhea due to the accumulation of unabsorbed sugars ...

Congenital Glucose-Galactose Malabsorption: A Case Report.
Last Updated: Nov 30, 2018

Congenital glucose-galactose malabsorption (CGGM) is a rare cause of intractable infantile diarrhea, with only a few hundred cases recognized worldwide. This life-threatening disorder must be considered in the differential diagnosis of an infant who presents with diarrhea and dehydration ...

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10 Free Research Articles 44 Research Articles