COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome
- PMID: 20488547
- PMCID: PMC3645485
- DOI: 10.1016/j.psychres.2010.04.048
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome
Abstract
The COMT gene is thought to contribute to the cognitive/psychiatric phenotypes in 22q11.2 deletion syndrome. We measured these manifestations against the Val/Met alleles of the COMT gene, in 40 nonpsychotic 22q11DS children. The Val allele was associated with poor IQ, processing speed, executive function and a higher frequency of anxiety disorders, underscoring the importance of the COMT gene in the childhood psychopathology in 22q11DS.
Copyright 2010 Elsevier Ireland Ltd. All rights reserved.
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