The treatment of phenylketonuria (PKU) patients constitutes a phenylalanine (Phe) intake restriction in their diet, which is achieved by adding a special Phe-free amino acid mixture to the diet. It has been reported that this diet could have some micronutrient deficiency. Several authors have also reported an increased oxidative stress or impaired antioxidant status in human and experimental PKU.
View Article and Find Full Text PDFJ Inherit Metab Dis
December 2008
Background: Discontinuation of dietary therapy in adults with phenylketonuria can lead to neuropsychological abnormalities and emotional problems. The aim of our study was to assess the change in quality of life in adult patients returning to the diet and to define the reasons for failure in diet resumption.
Methods: Quality of life was assessed by means of the Psychological General Well-Being Index before study entry and subsequently after 3 and 9 months.
Purpose: To find out if blood lead level (Pb-B) changes have influence on visual evoked potentials.
Material And Methods: 18 children (36 eyes) treated with CaNa2EDTA because of chronic environmental lead poisoning were examined two times: first at age 2-15.5 (mean 8) years and second 4 years later.
Purpose: The aim of this study is to find the relationship between lead level in blood (Pb-B) and visual evoked potentials (VEP) in children, environmentally exposed to lead.
Material And Methods: 32 children (64 eyes) with no clinical signs of lead poisoning were examined. Corrected visual acuity was 5/5 in all eyes.
Unlabelled: Malnutrition and loss of appetite remain a frequent problem in children with chronic renal failure (CRF). Recent studies in human gave much attention for leptin, polypeptide produced by adipocytes, and its influence on appetite and energetic balance regulation. The study aimed at evaluation of serum leptin levels (SLL) in children with CRF with regard to applied method of treatment.
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