Oliver Chris, Arron Kate, Sloneem Jenny, Hall Scott
Centre for Neurodevelopmental Disorders, School of Psychology, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Br J Psychiatry. 2008 Dec;193(6):466-70. doi: 10.1192/bjp.bp.107.044370.
Cornelia de Lange syndrome is associated with abnormalities on chromosomes 5, 10 and X.
To delineate the behavioural phenotype of Cornelia de Lange syndrome with specific reference to autistic-spectrum disorder.
A total of 54 individuals with Cornelia de Lange syndrome (mean age 13.88 years; s.d.=8.58) and 46 comparable individuals with intellectual disability (mean age 13.74 years; s.d.=7.99) were assessed on measures of autistic-spectrum disorder, and adaptive, compulsive and disordered behaviour.
There was no difference between the groups in global behaviour disorder. Severe autism was significantly more prevalent in the syndrome group (32.1%) than the comparison group (7.1%). In addition, the syndrome group also evidenced significantly higher levels of compulsive behaviour.
These data suggest that autistic-spectrum disorder is part of the behavioural phenotype of Cornelia de Lange syndrome and that compulsive behaviours are evident. Future research should investigate this behavioural phenotype using contemporary diagnostic algorithms for autism with detailed examination of the phenomenology of compulsive behaviours.
科妮莉亚·德朗格综合征与5号、10号和X染色体异常有关。
明确科妮莉亚·德朗格综合征的行为表型,特别提及自闭症谱系障碍。
对总共54名科妮莉亚·德朗格综合征患者(平均年龄13.88岁;标准差=8.58)和46名智力残疾对照个体(平均年龄13.74岁;标准差=7.99)进行了自闭症谱系障碍、适应性、强迫性和紊乱行为的评估。
两组在总体行为障碍方面没有差异。严重自闭症在综合征组(32.1%)中的患病率显著高于对照组(7.1%)。此外,综合征组的强迫行为水平也明显更高。
这些数据表明自闭症谱系障碍是科妮莉亚·德朗格综合征行为表型的一部分,且强迫行为明显。未来的研究应使用当代自闭症诊断算法对这种行为表型进行研究,并详细检查强迫行为的现象学。