Investigation of autistic features among individuals with mild to moderate Cornelia de Lange syndrome

被引:17
作者
Nakanishi, Mariko [1 ]
Deardorff, Matthew A. [2 ]
Clark, Dinah [2 ]
Levy, Susan E. [1 ,3 ]
Krantz, Ian [2 ,3 ]
Pipan, Mary [1 ,3 ]
机构
[1] Childrens Hosp Philadelphia, Div Child Dev Rehabil & Metab Dis, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
关键词
Cornelia de Lange syndrome (CdLS); autism; behavioral phenotype; NIPBL; SMC1A; SMC3; DIAGNOSTIC OBSERVATION SCHEDULE; BRACHMANN-DELANGE SYNDROME; BEHAVIORAL-PHENOTYPE; SPECTRUM DISORDERS; ADI-R; INTERVIEW; CHILDREN; VERSION;
D O I
10.1002/ajmg.a.34014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cornelia de Lange syndrome (CdLS) is a congenital disorder characterized by distinctive facial features, growth retardation, limb abnormalities, intellectual disability, and behavioral problems. Autism has been reported to occur frequently in CdLS, but the frequency of autism in individuals with the milder CdLS phenotype is not well studied. We investigated autistic features by using a screening tool and a diagnostic interview in 49 individuals with the mild to moderate phenotype from a CdLS research database at the Children's Hospital of Philadelphia. The Social Communication Questionnaire (SCQ), a screening instrument for autistic disorder, was completed for all individuals. For individuals who screened positive and a subset of those that screened negative, the Autism Diagnostic Interview-Revised (ADI-R) was administered. Autistic symptom severity was not significantly different by gender, age groups, and genotypes. There was a significant correlation between higher levels of adaptive functioning and lower scores of autistic symptoms. The estimated prevalence of significant autistic features by ADI-R criteria was 43% in our cohort of individuals with the mild to moderate CdLS phenotype, which suggests that prevalence of autistic disorder may be higher than previously described among individuals with mild to moderate phenotype of CdLS. Clinicians who take care of individuals with CdLS should have a high index of suspicion for autistic features, and refer for further evaluation when these features are present in order to expedite appropriate intervention. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1841 / 1847
页数:7
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