Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects

Autism has been reported in untreated patients with phenylketonuria. The authors aimed to explore autism in 15 Tunisian and 4 Algerian phenylketonuria patients, and report their clinical, biochemical and molecular peculiarities. The Childhood Autism Rating Scale and the Autism Diagnostic Interview–Revised were used for the diagnosis of autism. Five exons of phenylalanine hydroxylase gene (7, 6, 10, 11, and 5) were amplified by polymerase chain reaction and directly sequenced. Among these patients, 15 were suffering from autism at the time of evaluation. Six mutations were identified: p.E280K, p.G352Vfs, IVS10nt11, p.I224T, p.R261Q, and p.R252W. There was no correlation between autism and mutations affecting the phenylalanine hydroxylase gene, but the age of diet onset was the determining factor in autistic symptoms’ evolution.

Source: Journal of Child Neurology - May 10, 2016 Category: Neurology Authors: Khemir, S., Halayem, S., Azzouz, H., Siala, H., Ferchichi, M., Guedria, A., Bedoui, A., Abdelhak, S., Messaoud, T., Tebib, N., Belhaj, A., Kaabachi, N. Tags: Original Articles Source Type: research