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;
D O I
暂无
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
收藏
页码:921 / 923
页数:2
相关论文
共 50 条
  • [31] Connecting DCX, COMT and FMR1 in social behavior and cognitive impairment
    Delprato, Anna
    Xiao, Emily
    Manoj, Devika
    BEHAVIORAL AND BRAIN FUNCTIONS, 2022, 18 (01)
  • [32] Fragile X Syndrome in a Female With Homozygous Full-Mutation Alleles of the FMR1 Gene
    Vafaeie, Farzane
    Alerasool, Masoome
    Mojaver, Nasrin Kaseb
    Mojarrad, Majid
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (07)
  • [33] Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance
    Allen, EG
    Sherman, S
    Abramowitz, A
    Leslie, M
    Novak, G
    Rusin, M
    Scott, E
    Letz, R
    BEHAVIOR GENETICS, 2005, 35 (04) : 435 - 445
  • [34] Reduced vagal tone in women with the FMR1 premutation is associated with FMR1 mRNA but not depression or anxiety
    Klusek, Jessica
    LaFauci, Giuseppe
    Adayev, Tatyana
    Brown, W. Ted
    Tassone, Flora
    Roberts, Jane E.
    JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2017, 9
  • [35] Examination of the Effect of the Polymorphic CGG Repeat in the FMR1 Gene on Cognitive Performance
    Emily Graves Allen
    Stephanie Sherman
    Ann Abramowitz
    Mary Leslie
    Gloria Novak
    Michele Rusin
    Elizabeth Scott
    Richard Letz
    Behavior Genetics, 2005, 35 : 435 - 445
  • [36] Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation
    Bodega, B
    Bione, S
    Dalprà, L
    Toniolo, D
    Ornaghi, F
    Vegetti, W
    Ginelli, E
    Marozzi, A
    HUMAN REPRODUCTION, 2006, 21 (04) : 952 - 957
  • [37] The Behavioral Phenotype of FMR1 Mutations
    Boyle, Lia
    Kaufmann, Walter E.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2010, 154C (04) : 469 - 476
  • [38] Newborn screening and cascade testing for FMR1 mutations
    Sorensen, Page L.
    Gane, Louise W.
    Yarborough, Mark
    Hagerman, Randi J.
    Tassone, Flora
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (01) : 59 - 69
  • [39] Developmental aspects of FXAND in a man with the FMR1 premutation
    Santos, Ellery
    Emeka-Nwonovo, Chinelo
    Wang, Jun Yi
    Schneider, Andrea
    Tassone, Flora
    Hagerman, Paul
    Hagerman, Randi
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (02):
  • [40] FMR1: A gene with three faces
    Oostra, Ben A.
    Willemsen, Rob
    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2009, 1790 (06): : 467 - 477