Uridine diphosphate galactose 4-epimerase deficiency

Eur J Pediatr. 1981 Feb;135(3):303-4. doi: 10.1007/BF00442108.

Abstract

A case of uridine diphosphate galactose (UDP-Gal) 4-epimerase deficiency was discovered by mass screening of newborn infants. UDP-Gal 4-epimerase activity of red blood cells from the patient was found to be remarkably low, i.e., 7.5% of the level in normal controls at comparable ages. The parents showed intermediate values between those of the patient and controls. The enzyme activity in a specimen of liver tissue obtained from the patient by needle biopsy revealed a normal value. Subsequently, two other families with the condition were found by mass screening and these individuals were found to be heterozygotes.

Publication types

  • Case Reports

MeSH terms

  • Carbohydrate Epimerases / deficiency*
  • Carbohydrate Metabolism, Inborn Errors / diagnosis*
  • Carbohydrate Metabolism, Inborn Errors / epidemiology
  • Erythrocytes / enzymology
  • Humans
  • Infant
  • Japan
  • Liver / enzymology
  • Male
  • Mass Screening
  • Pedigree
  • UDPglucose 4-Epimerase / deficiency*

Substances

  • Carbohydrate Epimerases
  • UDPglucose 4-Epimerase