- Diet and metabolism studies
- Metabolism and Genetic Disorders
- Mitochondrial Function and Pathology
- Neonatal Health and Biochemistry
Hospital Universitario Virgen del Rocío
2018
In infants with phenylketonuria (PKU), dietary management is based on lowering and titrating phenylalanine (Phe) intake from breast milk or standard infant formula in combination a Phe-free order to maintain blood Phe levels within target range. Professionals use different methods feed PKU our survey aimed document practices across Europe.We sent cross sectional, monkey® questionnaire European health professionals working IMD. It contained 31 open multiple-choice questions. The results were...
In phenylketonuria (PKU), weaning is considered more challenging when compared to feeding healthy infants. The primary aim of gradually replace natural protein from breast milk or standard infant formula with solids containing equivalent phenylalanine (Phe). addition, a Phe-free second stage L-amino acid supplement usually recommended around 6 months formula. Our was assess different approaches used by health professionals across Europe. A cross sectional questionnaire (survey monkey®)...