Validation of Hagerman’s behavioral phenotype for fragile X syndrome among men with intellectual disability

Jacques Bellavance, M. Diane, Catherine Mello
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Abstract

Purpose The behavioral phenotype of fragile X syndrome (FXS) and intellectual disability (ID) proposed by Hagerman et al. (2009) was primarily based on data from male children and teens. The purpose of this study was to promote a better understanding of how this condition manifests in adults. Design/methodology/approach A total of 18 men of FXS were paired with men with Down syndrome on the basis of age and level of ID. A screening checklist was created on the basis of existing scales and the Hagerman et al. (2009) behavioral phenotype and completed by care providers. Findings Five of the 12 features of the phenotype were significantly more present among men with FXS than in men with Down syndrome. Originality/value This study provides partial confirmation for Hagerman et al.’s (2009) behavioral phenotype of FXS among men with moderate ID and identified some traits that warrant further investigation.
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智力残疾男性脆性X综合征Hagerman行为表型的验证
目的Hagerman等人(2009)提出的脆性X综合征(FXS)和智力残疾(ID)的行为表型主要基于男性儿童和青少年的数据。这项研究的目的是为了更好地了解这种情况在成年人中的表现。设计/方法/方法根据年龄和ID水平,共有18名FXS男性与唐氏综合征男性配对。在现有量表和Hagerman等人(2009)行为表型的基础上创建了筛查清单,并由护理人员完成。发现12个表型特征中有5个在患有FXS的男性中明显多于唐氏综合征的男性。原创性/价值本研究部分证实了Hagerman等人(2009)在中度ID男性中的FXS行为表型,并确定了一些值得进一步研究的特征。
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来源期刊
CiteScore
1.60
自引率
18.20%
发文量
22
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