Journal article

Detailed profile of cognitive dysfunction in children with aspartylglucosaminuria


Authors listHarjunen, Elina Leena; Laine, Minna; Tikkanen, Ritva; Helenius, Päivi

Publication year2020

Pages318-325

JournalJournal of Inherited Metabolic Disease

Volume number43

Issue number2

ISSN0141-8955

eISSN1573-2665

DOI Linkhttps://doi.org/10.1002/jimd.12159

PublisherSpringer


Abstract
Aspartylglucosaminuria (AGU) is a rare, recessively inherited lysosomal disease with relatively high prevalence in Finnish population. This progressive disease has a vast impact on patient's cognition and physical health, leading to intellectual disability and shorter life expectancy. Cognitive functions of 21 7- to 14-year-old children with AGU were studied cross-sectionally using Wechsler's Intelligence Scale for Children IV and the results were compared with a standardized Finnish sample. In addition to overall cognitive performance, abilities in discrete cognitive domains, including verbal comprehension, perceptual reasoning, working memory, and processing speed, were examined. The results showed that despite the very low overall level of cognitive performance, there were notable differences between individuals. All those children whose performance was closer to their own age level were 7 to 10 years old. Processing speed appeared more compromised, as compared with verbal comprehension. Furthermore, examining the subtest raw scores, there were no significant positive correlations between age and subtest scores, suggesting that the developmental level of AGU children could be rather stable throughout ages 7 to 14. This study gives insight to the severe nature of AGU disease. Since younger children performed better compared to their age norms than older children, the results raise a question whether the highest peak in cognitive functions is reached at an earlier age than previously thought.



Citation Styles

Harvard Citation styleHarjunen, E., Laine, M., Tikkanen, R. and Helenius, P. (2020) Detailed profile of cognitive dysfunction in children with aspartylglucosaminuria, Journal of Inherited Metabolic Disease, 43(2), pp. 318-325. https://doi.org/10.1002/jimd.12159

APA Citation styleHarjunen, E., Laine, M., Tikkanen, R., & Helenius, P. (2020). Detailed profile of cognitive dysfunction in children with aspartylglucosaminuria. Journal of Inherited Metabolic Disease. 43(2), 318-325. https://doi.org/10.1002/jimd.12159



Keywords


aspartylglucosaminuriaCOGNITIVE FUNCTIONSdisorder of glycoprotein degradationINTELLECTUAL DISABILITYLysosomal storage diseaseNEUROPSYCHOLOGY

Last updated on 2025-28-07 at 14:45