Neonatal diabetes mellitus with hypergalactosemia

Eur J Endocrinol. 1999 Oct;141(4):379-81. doi: 10.1530/eje.0.1410379.

Abstract

We report the case of a male, small-for-gestational-age newborn who presented with failure to thrive, severe fluctuation of blood glucose concentrations, and increased serum concentrations of galactose. The infant responded well to a lactose-free diet supplemented with fructose, inulin and corn starch. The metabolic disorder disappeared within 6 months. The transient course, and results of a molecular analysis of the glucose transporter 2 (Glut2) gene seem to rule out Fanconi-Bickel syndrome.

Publication types

  • Case Reports

MeSH terms

  • Diabetes Mellitus / blood*
  • Diabetes Mellitus / genetics
  • Diagnosis, Differential
  • Fanconi Syndrome / diagnosis
  • Galactose / blood*
  • Glucose Transporter Type 2
  • Humans
  • Infant, Newborn
  • Infant, Small for Gestational Age*
  • Male
  • Monosaccharide Transport Proteins / genetics

Substances

  • Glucose Transporter Type 2
  • Monosaccharide Transport Proteins
  • Galactose