Literature DB >> 22740374

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

Mariko Nakanishi1, Matthew A Deardorff, Dinah Clark, Susan E Levy, Ian Krantz, Mary Pipan.   

Abstract

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.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22740374      PMCID: PMC3557850          DOI: 10.1002/ajmg.a.34014

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  31 in total

1.  Neurologic and psychometric findings in the Brachmann-De Lange syndrome.

Authors:  A N Barr; J D Grabow; C G Matthews; F R Grosse; M L Motl; J M Opitz
Journal:  Neuropadiatrie       Date:  1971-07

2.  Brachmann-de Lange syndrome: diagnostic difficulties posed by the mild phenotype.

Authors:  R A Saul; R C Rogers; M C Phelan; R E Stevenson
Journal:  Am J Med Genet       Date:  1993-11-15

3.  de Lange syndrome: a clinical review of 310 individuals.

Authors:  L Jackson; A D Kline; M A Barr; S Koch
Journal:  Am J Med Genet       Date:  1993-11-15

4.  Brachmann-de Lange syndrome. Delineation of the clinical phenotype.

Authors:  M Ireland; D Donnai; J Burn
Journal:  Am J Med Genet       Date:  1993-11-15

5.  A behavioral phenotype in the de Lange syndrome.

Authors:  H G Johnson; P Ekman; W Friesen
Journal:  Pediatr Res       Date:  1976-10       Impact factor: 3.756

6.  Psycho-social assessment of 36 de Lange patients.

Authors:  B Beck
Journal:  J Ment Defic Res       Date:  1987-09

Review 7.  Autism spectrum disorders in genetic syndromes: implications for diagnosis, intervention and understanding the wider autism spectrum disorder population.

Authors:  J Moss; P Howlin
Journal:  J Intellect Disabil Res       Date:  2009-08-25

8.  Developmental data on individuals with the Brachmann-de Lange syndrome.

Authors:  A D Kline; C Stanley; J Belevich; K Brodsky; M Barr; L G Jackson
Journal:  Am J Med Genet       Date:  1993-11-15

9.  Mild Brachmann-de Lange syndrome. Phenotypic and developmental characteristics of mildly affected individuals.

Authors:  J B Moeschler; J M Graham
Journal:  Am J Med Genet       Date:  1993-11-15

10.  Interrelationship between Autism Diagnostic Observation Schedule-Generic (ADOS-G), Autism Diagnostic Interview-Revised (ADI-R), and the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) classification in children and adolescents with mental retardation.

Authors:  Annelies de Bildt; Sjoerd Sytema; Cees Ketelaars; Dirk Kraijer; Erik Mulder; Fred Volkmar; Ruud Minderaa
Journal:  J Autism Dev Disord       Date:  2004-04
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  10 in total

1.  Executive functioning in Cornelia de Lange syndrome: domain asynchrony and age-related performance.

Authors:  Donna Reid; Jo Moss; Lisa Nelson; Laura Groves; Chris Oliver
Journal:  J Neurodev Disord       Date:  2017-08-15       Impact factor: 4.025

2.  Cornelia de Lange syndrome: Correlation of brain MRI findings with behavioral assessment.

Authors:  Tamanna R Roshan Lal; Mark A Kliewer; Thelma Lopes; Susan L Rebsamen; Julia O'Connor; Marco A Grados; Amy Kimball; Julia Clemens; Antonie D Kline
Journal:  Am J Med Genet C Semin Med Genet       Date:  2016-05-10       Impact factor: 3.908

Review 3.  Behavioral and psychiatric manifestations in Cornelia de Lange syndrome.

Authors:  Marco A Grados; Mustafa H Alvi; Siddharth Srivastava
Journal:  Curr Opin Psychiatry       Date:  2017-03       Impact factor: 4.741

4.  A Case Report of Cornelia De Lange Syndrome in Northern Iran; A Clinical and Diagnostic Study.

Authors:  Seyyed-Mohsen Hosseininejad; Behnaz Bazrafshan; Ehsan Alaee
Journal:  J Clin Diagn Res       Date:  2016-02-01

5.  Cornelia de Lange and Ehlers-Danlos: comorbidity of two rare syndromes.

Authors:  Cora Cravero; Vincent Guinchat; Stéphane Barete; Angèle Consoli
Journal:  BMJ Case Rep       Date:  2016-02-01

6.  Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3.

Authors:  Elena Infante; Gorka Alkorta-Aranburu; Areeg El-Gharbawy
Journal:  Clin Case Rep       Date:  2017-06-28

7.  Decreased cohesin in the brain leads to defective synapse development and anxiety-related behavior.

Authors:  Yuki Fujita; Koji Masuda; Masashige Bando; Ryuichiro Nakato; Yuki Katou; Takashi Tanaka; Masahiro Nakayama; Keizo Takao; Tsuyoshi Miyakawa; Tatsunori Tanaka; Yukio Ago; Hitoshi Hashimoto; Katsuhiko Shirahige; Toshihide Yamashita
Journal:  J Exp Med       Date:  2017-04-13       Impact factor: 14.307

8.  Behavioral Phenotype and Autism Spectrum Disorders in Cornelia de Lange Syndrome.

Authors:  Lucia Parisi; Teresa Di Filippo; Michele Roccella
Journal:  Ment Illn       Date:  2015-09-30

Review 9.  Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement.

Authors:  Antonie D Kline; Joanna F Moss; Angelo Selicorni; Anne-Marie Bisgaard; Matthew A Deardorff; Peter M Gillett; Stacey L Ishman; Lynne M Kerr; Alex V Levin; Paul A Mulder; Feliciano J Ramos; Jolanta Wierzba; Paola Francesca Ajmone; David Axtell; Natalie Blagowidow; Anna Cereda; Antonella Costantino; Valerie Cormier-Daire; David FitzPatrick; Marco Grados; Laura Groves; Whitney Guthrie; Sylvia Huisman; Frank J Kaiser; Gerritjan Koekkoek; Mary Levis; Milena Mariani; Joseph P McCleery; Leonie A Menke; Amy Metrena; Julia O'Connor; Chris Oliver; Juan Pie; Sigrid Piening; Carol J Potter; Ana L Quaglio; Egbert Redeker; David Richman; Claudia Rigamonti; Angell Shi; Zeynep Tümer; Ingrid D C Van Balkom; Raoul C Hennekam
Journal:  Nat Rev Genet       Date:  2018-10       Impact factor: 53.242

10.  An Observational Study of Social Interaction Skills and Behaviors in Cornelia de Lange, Fragile X and Rubinstein-Taybi Syndromes.

Authors:  Katherine Ellis; Chris Oliver; Chrysi Stefanidou; Ian Apperly; Jo Moss
Journal:  J Autism Dev Disord       Date:  2020-11
  10 in total

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