Glucose-Galactose Malabsorption
Pedigree
Diagnosticstrategy
Forms
Print page
Sprachewechseln
Clinical feature:
Definition: Glucose-Galactose Malabsorption is an autosomal recessive disorder characterized by reduced intestinal resoption of glucose and galactose. The accompanying renal symptom is glucosuria.
Systematic link table:
Literature:
Turk E et al. (1991) Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter. Wright EM et al. (1991) Molecular genetics of intestinal glucose transport.
