Glucose-Galactose Malabsorption Deficiency Latest Advances
Find the Latest Research About Glucose-Galactose Malabsorption Deficiency
Last Updated: 06/30/2026
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Found 163 publications
Congenital glucose-galactose malabsorption due to SLC5A1 mutation: A case of hypernatraemic dehydration.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: May 20, 2026
A Rare Case of Congenital Glucose Galactose Malabsorption Due to SLC5A1 Mutation.
Journal: Cureus
Published: November 30, 2025
Congenital Glucose-Galactose Malabsorption: A Rare Cause of Intractable Diarrhea in Infancy.
Journal: Indian pediatrics
Published: May 01, 2025
A new link between insulinoma and congenital glucose-galactose malabsorption.
Journal: Endocrine oncology (Bristol, England)
Published: March 24, 2025
Congenital glucose-galactose malabsorption: An unusual cause of chronic diarrhea in infancy.
Journal: Revista de gastroenterologia de Mexico (English)
Published: March 24, 2025
Cracking the Codes for Congenital Diarrhea and Enteropathies (CoDEs): A Case Report and Review.
Journal: Cureus
Published: November 11, 2024
Renal glucosuria in children.
Journal: World journal of clinical pediatrics
Published: December 31, 2023
Congenital Diarrhoea In A Neonate With Hypernatraemia And Dehydration.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: November 28, 2023
Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose-galactose transporter SLC5A1.
Journal: Frontiers in pediatrics
Published: August 28, 2023
Congenital Glucose-Galactose Malabsorption in a Neonate with Hyperbilirubinemia and Hypernatremia.
Journal: Indian journal of pediatrics
Published: January 19, 2023
Last Updated: 06/30/2026