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Working memory and arithmetic impairments in children with FMR1 premutation and gray zone alleles

Expansive mutations in familial mental retardation 1 (FMR1) gene have been associated with different phenotypes. Full mutations are associated with intellectual disability and autism spectrum disorder; premutations are associated with math learning difficulties and working memory impairments. In gra...

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Detalles Bibliográficos
Autores principales: Martins, Aline Aparecida Silva, Paiva, Giulia Moreira, Matosinho, Carolina Guimarães Ramos, Coser, Elisângela Monteiro, Fonseca, Pablo Augusto de Souza, Haase, Vitor Geraldi, Carvalho, Maria Raquel Santos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academia Brasileira de Neurologia, Departamento de Neurologia Cognitiva e Envelhecimento 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170264/
https://www.ncbi.nlm.nih.gov/pubmed/35719251
http://dx.doi.org/10.1590/1980-5764-DN-2021-0035
Descripción
Sumario:Expansive mutations in familial mental retardation 1 (FMR1) gene have been associated with different phenotypes. Full mutations are associated with intellectual disability and autism spectrum disorder; premutations are associated with math learning difficulties and working memory impairments. In gray zone, neuropsychological development has not yet been described. OBJECTIVES: This study aimed to describe the frequency of FMR1 premutation and gray zone alleles in a school population sample representing a broad spectrum of variation in math achievement and detail school achievement and cognitive performance in the children identified with FMR1 premutation or gray zone alleles. METHODS: We described a two-phase study. In the first phase, 2,195 school-age children were screened for math achievement. In the second phase, 378 children with normal intelligence were neuropsychologically assessed and genotyped for FMR1. Of these, 121 children (61 girls) performed below percentile 25 in mathematics (MD group) and 257 children (146 girls) performed above percentile 25 (control group). RESULTS: Four pupils presented expanded alleles, one premutation and three gray zone alleles. The girl with the premutation and one boy with a gray zone allele presented impairments in working memory and arithmetic performance below percentile 6, compatible with the diagnosis of developmental dyscalculia. These children’s difficulties were not associated with inaccuracy of nonsymbolic number representations or literacy impairments. Dyscalculia in these children seems to be associated mainly with working memory impairments. CONCLUSIONS: FMR1 expansions in the gray zone may contribute to dyscalculia in otherwise healthy and normally intelligent children.