Swillen A, Devriendt K, Ghesquière P, Fryns J P
Center for Human Genetics Leuven, Clinical Genetics Unit, University of Leuven, Belgium.
Genet Couns. 2001;12(4):309-17.
Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school age: Common behavioral features described in children with the Velo-Cardio-Facial syndrome (VCFS) (del 22q11) are problems with attention and concentration, extremes in behavior and social problems, especially in relationship with peers. At present, it is unclear whether these behavioral manifestations are directly related to the chromosomal anomaly or related to other manifestations of the syndrome such as developmental delay and speech-language delay. This study describes for the first time the behavior of young primary school aged children with a del22q11 compared to a control group of children matched for age, sex and mental level, with similar developmental problems (speech-language impairment plus learning disability: SLI + LD) but without a del22q11 or any other known genetic condition. Parents and teachers evaluated the children's behavior with standardized questionnaires (CBCL; TRF). Results indicate that most of the behaviors are similar across both groups. The only differences found are in the field of <
患有22q11缺失的儿童与患有语言障碍和学习障碍的儿童:小学阶段的行为表现:腭心面综合征(VCFS,22q11缺失)患儿常见的行为特征包括注意力不集中、行为极端以及社交问题,尤其是与同龄人相处时。目前尚不清楚这些行为表现是直接与染色体异常相关,还是与该综合征的其他表现如发育迟缓及语言发育迟缓有关。本研究首次描述了患有22q11缺失的小学低年级儿童与一组年龄、性别和智力水平匹配的对照组儿童的行为表现,对照组儿童有类似的发育问题(语言障碍加学习障碍:SLI + LD),但没有22q11缺失或任何其他已知的遗传疾病。家长和教师通过标准化问卷(CBCL;TRF)对儿童的行为进行评估。结果表明,两组儿童的大多数行为表现相似。唯一发现的差异在于“退缩行为”和“攻击行为”方面。患有22q11缺失的儿童有更强的回避他人的倾向,而患有SLI + LD的儿童似乎更具攻击性。