Intermediate and expanded FMR1 alleles in an autistic Costa Rican population

被引:0
作者
Vindas-Smith, Rebeca [1 ]
Sequeira-Cordero, Andrey [1 ]
Castro-Volio, Isabel [1 ]
Jimenez-Gonzalez, Patricia [2 ]
Cuenca, Patricia [1 ]
Saborio-Rocafort, Manuel [2 ]
Fallas, Marietha [2 ]
Vasquez, Melissa [1 ]
机构
[1] Univ Costa Rica, Inst Invest Salud, San Jose, Costa Rica
[2] Hosp Nacl Ninos Dr Carlos Saenz Herrera, Caja Costarricense Seguro Social, San Jose, Costa Rica
来源
REVISTA MEXICANA DE NEUROCIENCIA | 2022年 / 23卷 / 02期
关键词
Autism spectrum disorder; Fragile X syndrome; Intermediate allele; Expanded allele; FMR1; FRAGILE-X-SYNDROME; CGG-REPEAT; FRAXA; GENE; EXPANSION; DISEASE; NUMBER; MALES; ZONE;
D O I
10.24875/RMN.21000044
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 (chi(2) 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.
引用
收藏
页码:51 / 56
页数:6
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