Breastfeeding in phenylketonuria

Acta Paediatr Suppl. 1999 Dec;88(432):25-7. doi: 10.1111/j.1651-2227.1999.tb01151.x.

Abstract

Eighty-three infants with classical phenylketonuria have been born in Norway since 1979. The treatment of these children is centralized at the National Hospital in Oslo. Seventy-four have been breastfed in combination with a phenylalanine-free protein substitute. Dietary treatment was commenced in hospital between 5 and 33 d of age (mean 14 d). Normalization of serum phenylalanine (below 400 pmol/l) took between 1 and 35 d (mean 8 d). The period of breastfeeding lasted from 1 to 16 mo (mean 7 mo). Growth (weight, length and head circumference) fell within the normal range for age on the Norwegian growth chart.

Publication types

  • Clinical Trial

MeSH terms

  • Breast Feeding*
  • Child Development / physiology
  • Female
  • Follow-Up Studies
  • Humans
  • Infant Food*
  • Infant Nutritional Physiological Phenomena
  • Infant, Newborn
  • Male
  • Norway
  • Phenylalanine / blood*
  • Phenylketonurias / blood
  • Phenylketonurias / diagnosis
  • Phenylketonurias / diet therapy*
  • Treatment Outcome

Substances

  • Phenylalanine