De Smedt B, Devriendt K, Fryns J-P, Vogels A, Gewillig M, Swillen A
Centre for Disability, Special Needs Education and Child Care, and Centre for Human Genetics, University of Leuven, Belgium.
J Intellect Disabil Res. 2007 Sep;51(Pt 9):666-70. doi: 10.1111/j.1365-2788.2007.00955.x.
Learning disabilities are one of the most consistently reported features in Velo-Cardio-Facial Syndrome (VCFS). Earlier reports on IQ in children with VCFS were, however, limited by small sample sizes and ascertainment biases. The aim of the present study was therefore to replicate these earlier findings and to investigate intellectual abilities in a large sample of children with VCFS. In addition, we aimed to identify factors that may contribute to within-syndrome variability in cognitive performance, such as the mode of inheritance of the deletion, sex, the presence of a heart defect and psychiatric morbidity.
IQ data of 103 children with VCFS (56 males, 47 females) were collected. Psychiatric diagnosis was additionally recorded.
Children with VCFS had a mean full-scale IQ (FSIQ) of 73.48 (range: 50-109). There were no effects of sex, presence of a heart defect and psychiatric condition on intellectual profile. Inheritance of the deletion affected cognitive performance in VCFS, with children with familial deletions having significant lower FSIQ than children with a de novo deletion.
Learning disabilities are very common in children with VCFS, although marked within syndrome variability is noted. One factor contributing to this variability seems to be the mode of inheritance of the deletion.
学习障碍是腭心面综合征(VCFS)中最常被报告的特征之一。然而,早期关于VCFS患儿智商的报告受到样本量小和确定偏倚的限制。因此,本研究的目的是重复这些早期发现,并在一大群VCFS患儿中研究智力能力。此外,我们旨在确定可能导致综合征内认知表现差异的因素,如缺失的遗传模式、性别、心脏缺陷的存在和精神疾病发病率。
收集了103名VCFS患儿(56名男性,47名女性)的智商数据。此外还记录了精神疾病诊断情况。
VCFS患儿的平均全量表智商(FSIQ)为73.48(范围:50 - 109)。性别、心脏缺陷的存在和精神疾病状况对智力概况没有影响。缺失的遗传影响了VCFS的认知表现,家族性缺失患儿的FSIQ显著低于新发缺失患儿。
学习障碍在VCFS患儿中非常常见,尽管综合征内存在明显差异。导致这种差异的一个因素似乎是缺失的遗传模式。