Eighty-seven participants of the German Collaboratory Study for Childr
en with Phenylketonuria (PKU) presented low plasma, whole blood and ha
ir selenium (Se) values, reduced urinary selenium excretion, and decre
ased plasma and erythrocyte glutathione peroxidase activity in compari
son with a healthy reference group (all figures p < 0.001). Aspartate
amino transferase and thyroxine (T-4) concentrations in plasma were in
versely correlated with the selenium blood values of the PKU children.
Somatic measurements showed a negative standard deviation score of bo
dy height in the PKU children compared with reference values. Despite
the different Se supply, the infants did not present any specific Se d
eficiency symptoms.