Nutrient intakes of adolescents with phenylketonuria and infants and children with maple syrup urine disease on semisynthetic diets.
- 1 April 1993
- journal article
- research article
- Published by Taylor & Francis in Journal of the American College of Nutrition
- Vol. 12 (2) , 108-114
- https://doi.org/10.1080/07315724.1993.10718290
Abstract
Adequacy of nutrient intakes of adolescents with and without phenylketonuria (PKU) and infants and children with and without maple syrup urine disease (MSUD) were assessed using 3-day diet records sorted by disease and by age of the subject. Mean intakes of all nutrients were greater than two-thirds of the Recommended Dietary Allowances (RDA) or Estimated Safe and Adequate Daily Dietary Intakes (ESADDI) for all adolescents studied, with the exception of selenium (Se) in PKU adolescents, which averaged 27.8 micrograms. For adolescents with PKU, > 50% of the RDA or ESADDI for all nutrients was provided by elemental or modified protein hydrolysate medical foods, except for vitamin A in children aged 11-15 years and Se in children 11-18 years. Mean nutrient intakes of all infants and children were greater than two-thirds of the RDA or ESADDI for all nutrients except Se in MSUD children aged 1-11 years, where intakes ranged from 6.4 to 13.2 micrograms (21-66% of the RDA). The medical foods provided for most of the RDA and ESADDI recommendations, with the exception of Se in MSUD children.Keywords
This publication has 16 references indexed in Scilit:
- Tyrosine- and phenylalanine-restricted formula diet augments immunocompetence in healthy humansThe American Journal of Clinical Nutrition, 1990
- Trace Element Status of PKU Children Ingesting an Elemental DietJournal of Parenteral and Enteral Nutrition, 1987
- Problems related to diet management of maternal phenylketonuriaJournal of Inherited Metabolic Disease, 1986
- Study of serum ferritin in 58 children with classic phenylketonuria and persistent hyperphenylalaninaemiaJournal of Inherited Metabolic Disease, 1985
- Plasma selenium levels in treated phenylketonuric patientsJournal of Inherited Metabolic Disease, 1985
- The effect of treatment on zinc, copper and calcium status in children with phenylketonuriaJournal of Inherited Metabolic Disease, 1984
- Zinc and Copper Status of Treated Children with PhenylketonuriaJournal of Parenteral and Enteral Nutrition, 1981
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic DisordersAnnals of Nutrition and Metabolism, 1977
- Zinc nutrition of preschool children in the Denver Head Start programThe American Journal of Clinical Nutrition, 1976
- Serum-selenium concentrations in patients with maple-syrup-urine disease and phenylketonuria under dieto-therapyClinica Chimica Acta; International Journal of Clinical Chemistry, 1975