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PMID: 35381410 Published · ppublish English

Visual-processing deficits in children with neurofibromatosis type 1: A clinical marker of reading difficulties.

Vernet M, Jover M, Bellocchi S, Maziero S, Jucla M, Tallet J, Danna J, Chaix Y, Ducrot S

Abstract

Today's estimates indicate that nearly 50% of children with Neurofibromatosis type 1 (NF1) suffer from reading disabilities, with a high impact on their academic achievement. In addition to the well-documented importance of phonological skills in reading acquisition and neurodevelopmental disorders, visual-attention processes also appear as important factors in learning to read. The present study aimed at assessing the role of visual-processing dysfunction in the high prevalence of reading disabilities in NF1 children and providing a useful tool for clinician in the early detection of reading impairment in this neurogenetic disorder. Forty-two children with NF1 and 42 typically developing children (TD) participated in the study. All were right-handed and did not present intellectual disability or attention deficit hyperactivity disorder. Visual-attention processes were assessed with the Developmental Eye Movement (DEM) test, together with the NF1 children's reading level. NF1 children with and without reading disabilities were then compared. The results showed that visual-processing deficits were highly present among the NF1 children included in our study. Furthermore, poor readers with NF1 presented an increased risk of visual-processing deficits compared to peers. This finding supports the role of visual-processing deficits in the reading difficulties encountered in nearly half of children with NF1. Finally, in NF1 children without intellectual or attention disability, visual-processing deficits emerge as one of the clinical markers of reading disabilities. The study holds important clinical implications both for the identification, by providing a useful screening tool, and the management of reading disabilities in NF1 children.

Keywords
DEM-Test Neurofibromatosis type 1 Reading Screening tool Visual information processing
MeSH 主题词
Biomarkers Child Cognition Dyslexia/diagnosis,etiology Humans Learning Disabilities/diagnosis,epidemiology Neurofibromatosis 1/complications
Article Info
Journal
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Abbr.
Eur J Paediatr Neurol
ISSN
1532-2130
Corresponding email
Published
2022-05-00
Language
English
Country/Region
England
NLM ID
9715169
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