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Glucose-galactose malabsorption
What is Glucose-galactose malabsorption?
Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period.
Other condition names
SGLT1 deficiency
Inheritance type
Autosomal recessive
Prevalence
Worldwide: Unknown
Age of Onset
Infancy
Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on
"https://www.orphadata.com"
. Data version 1.3.16 / 4.1.7.