Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2946
Title: Executive functioning of 4 children with hyperphenylalaninemia from childhood to adolescence
Authors: McGill, J.
Jones, T.
Sullivan, K. A.
Sharman, R.
Young, R. M.
Issue Date: 2015
Source: 135, (4), 2015, p. e1072-e1074
Pages: e1072-e1074
Journal: Pediatrics
Abstract: Hyperphenylalaninemia is a variant of phenylketonuria, and debate remains as to what, if any, active management of this condition is required to preserve cognitive function and psychological well-being. This study is the first to examine longitudinally the executive function (EF) in adolescents with hyperphenylalaninemia. Two sibling pairs with mild hyperphenylalaninemia underwent neuropsychological examination in early childhood and again in adolescence using EF tests that were highly sensitive to phenylalanine exposure. By early adolescence, none of the 4 children demonstrated EF impairment. The children demonstrated a typical developmental trajectory of EF from childhood to adolescence, given phenylalanine exposure consistent with their condition.L6038366322015-04-23
2015-04-28
DOI: 10.1542/peds.2013-4200
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L603836632&from=exporthttp://dx.doi.org/10.1542/peds.2013-4200 |
Keywords: Australia;child;childhood disease;clinical article;cognitive defect;diet supplementation;executive function;female;follow up;human;hyperphenylalaninemia;infant;tyrosine;male;neuropsychological assessment II;preschool child;priority journal;protein restriction;Rey Osterreith complex figure test;Stroop test;Wechsler intelligence scale;phenylalanineprotein;longitudinal study;adolescent;article;assessment of humans
Type: Article
Appears in Sites:Children's Health Queensland Publications

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