Genetics reference · Gastroenterology
Glucose-galactose malabsorption
MedlinePlus Genetics, National Library of Medicine · Retrieved 2026-10-13
Glucose-galactose malabsorption is a condition in which the body cannot take in (absorb) the sugars glucose and galactose, which primarily results in severe diarrhea. Beginning in infancy, severe diarrhea results in weight loss and dehydration that can be life-threatening. Small amounts of the simple sugar glucose in the urine (mild glucosuria) may occur in this disorder. Rarely, affected infants develop kidney stones due to deposits of calcium in the kidneys…
Reference details
- Inheritance patterns
- Autosomal recessive
- Other names
- Carbohydrate intolerance; Complex carbohydrate intolerance; Congenital glucose-galactose intolerance; Congenital glucose-galactose malabsorption; GGM; Monosaccharide malabsorption
- NLM review date
- 2020-04
- NLM publication date
- 2020-08-18
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Source date: 2020-04. Retrieved: 2026-10-13. Text has been organized for reading; this import has not been independently reviewed by a clinician. It is not individualized medical advice.
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