Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes

被引:0
作者
Irene Madrigal
Mar Xunclà
Maria Isabel Tejada
Francisco Martínez
Isabel Fernández-Carvajal
Luís Alberto Pérez-Jurado
Laia Rodriguez-Revenga
Montserrat Milà
机构
[1] Hospital Clínic,CIBER de Enfermedades Raras and Biochemistry and Molecular Genetics Department
[2] Fundació Clinic per a la Recerca Biomèdica,Biochemistry Department
[3] Molecular Genetics Laboratory,undefined
[4] Cruces Hospital,undefined
[5] GIRMOGEN (Spanish Network for Mental Retardation),undefined
[6] Spain,undefined
[7] Unidad de Genética,undefined
[8] Hospital Universitario La Fe,undefined
[9] Instituto de Biología y Genética Molecular (IBGM),undefined
[10] Universidad de Valladolid,undefined
[11] Centro Superior de Investigaciones Científicas (CSIC),undefined
[12] CIBER de Enfermedades Raras,undefined
[13] Genetics Unit,undefined
[14] Universitat Pompeu Fabra,undefined
[15] Program in Molecular Medicine,undefined
[16] Institut d’Investigacions Biomèdiques August Pi i Sunyer,undefined
来源
European Journal of Human Genetics | 2011年 / 19卷
关键词
intermediate alleles; cognitive and behavioural phenotypes; FMR1; ASD; ADHD;
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中图分类号
学科分类号
摘要
During the last few years, several studies have reported an excess of intermediate FMR1 alleles in patients with cognitive and/or behavioural phenotypes. Here, we report the frequency of intermediate alleles (IAs) in three pathologies, intellectual disabilities (IDs), attention-deficit/hyperactivity disorder and autism, from different Spanish regions. We found 142 IAs among 9015 patients with ID (1.6%), 4 among the 415 ADHD patients (0.96%) and 4 among the 300 autistic patients (1.3%), similar to the frequency reported in our control population. No evidence was found of an excess of IA at the FRAXA locus in any of the study populations, although geographical variability was detected. Moreover, the analysis of 100 transmissions of IAs showed that 95% of these alleles were stable. Only 3% expanded within the same range and 2% expanded to a full mutation in two generations. No evidence of an association between IAs and behavioural or cognitive phenotypes was found, suggesting that IAs are not clearly implicated in these pathologies.
引用
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页码:921 / 923
页数:2
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