Intermediate and expanded FMR1 alleles in an autistic Costa Rican population

 

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Autores: Vindas Smith, Rebeca, Sequeira Cordero, Andrey, Castro Volio, Isabel, Jiménez González, Patricia, Cuenca Berger, Patricia, Saborío Rocafort, Manuel, Fallas Delgado, Marietha, Vásquez Cerdas, Melissa
Formato: artículo original
Data de Publicação:2022
Descrição:Objective: We aimed to determine the distribution of intermediate and expanded FMR1 alleles in Costa Rican individuals diagnosed with autism. Materials and methods: A total of 212 autism spectrum disorder (ASD) cases of Costa Rican individuals and 943 male newborn controls were screened by means of polymerase chain reaction to determine the frequency of intermediate, premutation, and full mutation FMR1 alleles. Full mutation suspected cases were confirmed by Southern blot analyses. Frequencies of FMR1 alleles in the case group were compared with frequencies observed in a population-based sample of male newborn controls. Results: A significant excess of intermediate allele carriers was found in ASD individuals as compared to controls (χ2 test, p < 0.001). Four, out of 188 males in the case group, were identified as full mutation carriers. Conclusions: Our results suggest a possible involvement of the gray zone or intermediate alleles in ASD.
País:Kérwá
Recursos:Universidad de Costa Rica
Repositorio:Kérwá
Idioma:Inglés
OAI Identifier:oai:kerwa.ucr.ac.cr:10669/85932
Acesso em linha:https://www.revmexneurociencia.com/frame_esp.php?id=171
https://hdl.handle.net/10669/85932
Palavra-chave:Autism spectrum disorder
Fragile X syndrome
Intermediate allele
Expanded allele
FMR1
Trastorno del espectro autista
Síndrome del cromosoma X frágil
Alelo intermedio
Alelo expandido