哥斯达黎加自闭症人群中FMR1的中间和扩展等位基因

IF 0.5 Q4 CLINICAL NEUROLOGY
Rebeca Vindas-Smith, Andrey Sequeira-Cordero, I. Castro-Volio, Patricia Jiménez-González, P. Cuenca, Manuel Saborio-Rocafort, Marietha Fallas, Melissa Vásquez
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引用次数: 1

摘要

目的:我们旨在确定中间和扩增的FMR1等位基因在被诊断为自闭症的哥斯达黎加个体中的分布。材料和方法:通过聚合酶链式反应筛选212例哥斯达黎加个体和943例男性新生儿对照的自闭症谱系障碍(ASD)病例,以确定中间突变、预突变和全突变FMR1等位基因的频率。Southern印迹分析证实了完全突变的疑似病例。将病例组中FMR1等位基因的频率与基于人群的男性新生儿对照样本中观察到的频率进行比较。结果:与对照组相比,ASD患者的中间等位基因携带者显著增多(χ2检验,p<0.001)。病例组188名男性中有4名被确定为完全突变携带者。结论:我们的研究结果提示ASD可能涉及灰色带或中间等位基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermediate and expanded FMR1 alleles in an autistic Costa Rican population
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 ( χ 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.
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来源期刊
Revista Mexicana de Neurociencia
Revista Mexicana de Neurociencia CLINICAL NEUROLOGY-
自引率
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发文量
28
审稿时长
28 weeks
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