Forty-three adults with classical phenylketonuria were identified by n
eonatal screening and treated with a phenylalanine (Phe) restricted di
et. Nineteen have remained on dietary treatment with varying levels of
blood Phe control and 24 have discontinued the diet at an average age
of 7.8 years. Follow up at an average age of 22 years revealed that t
he cohort remaining on dietary treatment have achieved substantially b
etter social and academic achievement than the 24 who discontinued die
tary treatment. Another group of 19 adults who were not diagnosed unti
l an average age of 2.5 years have also been evaluated after an averag
e of 22 years on a Phe restricted diet. This report is based upon Wech
sler Adult Intelligence Revised Test scores, attendance at college, em
ployment and marital status.