Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene

Dig Dis Sci. 2017 Jan;62(1):280-281. doi: 10.1007/s10620-016-4348-2. Epub 2016 Oct 25.
No abstract available

Keywords: Glucose–galactose malabsorption; Neonatal diarrhea; SLC5A1.

Publication types

  • Case Reports

MeSH terms

  • Carbohydrate Metabolism, Inborn Errors / diagnosis*
  • Carbohydrate Metabolism, Inborn Errors / genetics*
  • Humans
  • Infant, Newborn
  • Malabsorption Syndromes / diagnosis*
  • Malabsorption Syndromes / genetics*
  • Male
  • Mutation / genetics*
  • Sodium-Glucose Transporter 1 / genetics*
  • Turkey

Substances

  • SLC5A1 protein, human
  • Sodium-Glucose Transporter 1

Supplementary concepts

  • Glucose-Galactose Malabsorption