Literature DB >> 12072882

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).

Bronwyn Glaser1, Donna L Mumme, Christine Blasey, Michael A Morris, Sophie P Dahoun, Stylianos E Antonarakis, Allan L Reiss, Stephan Eliez.   

Abstract

OBJECTIVE: To further define the language profile of children with velocardiofacial syndrome (VCFS) and explore the influence of parental origin of the deletion on language. STUDY
DESIGN: Children and adolescents with VCFS (n = 27) were group-matched for sex, age, and IQ with 27 children and adolescents with idiopathic developmental delay. Fifty-four typically developing control subjects were also included in the analyses investigating word association abilities.
RESULTS: Children with VCFS had significantly lower receptive than expressive language skills, a unique finding when compared with IQ-matched control subjects. However, no significant differences in word association were detected. Children with a deletion of paternal origin score significantly higher on receptive language when compared with children with a deletion of maternal origin.
CONCLUSIONS: The Clinical Evaluation of Language Fundamentals-III results suggest that children with VCFS show more severe deficits in receptive than expressive language abilities. Language skills of children with VCFS could be influenced by parental origin of the deletion and thus related to neuroanatomic alterations at the deletion site.

Entities:  

Mesh:

Year:  2002        PMID: 12072882     DOI: 10.1067/mpd.2002.124774

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  19 in total

Review 1.  Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome.

Authors:  Kerri L Tang; Kevin M Antshel; Wanda P Fremont; Wendy R Kates
Journal:  J Dev Behav Pediatr       Date:  2015-10       Impact factor: 2.225

Review 2.  The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

Authors:  Rachel K Jonas; Caroline A Montojo; Carrie E Bearden
Journal:  Biol Psychiatry       Date:  2013-08-28       Impact factor: 13.382

Review 3.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

4.  No evidence for parental imprinting of mouse 22q11 gene orthologs.

Authors:  Thomas M Maynard; Daniel W Meechan; Clifford C Heindel; Amanda Z Peters; Robert M Hamer; Jeffrey A Lieberman; Anthony-Samuel LaMantia
Journal:  Mamm Genome       Date:  2006-08-04       Impact factor: 2.957

5.  Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

Authors:  Kevin M Antshel; Alka Aneja; Leslie Strunge; Jena Peebles; Wanda P Fremont; Kimberly Stallone; Nuria Abdulsabur; Anne Marie Higgins; Robert J Shprintzen; Wendy R Kates
Journal:  J Autism Dev Disord       Date:  2006-12-19

6.  Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.

Authors:  Wendy R Kates; Ravi Bansal; Wanda Fremont; Kevin M Antshel; Xuejun Hao; Anne Marie Higgins; Jun Liu; Robert J Shprintzen; Bradley S Peterson
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2011-01-14       Impact factor: 8.829

Review 7.  22q11.2 deletion syndrome.

Authors:  Donna M McDonald-McGinn; Kathleen E Sullivan; Bruno Marino; Nicole Philip; Ann Swillen; Jacob A S Vorstman; Elaine H Zackai; Beverly S Emanuel; Joris R Vermeesch; Bernice E Morrow; Peter J Scambler; Anne S Bassett
Journal:  Nat Rev Dis Primers       Date:  2015-11-19       Impact factor: 52.329

8.  Factors affecting articulation skills in children with velocardiofacial syndrome and children with cleft palate or velopharyngeal dysfunction: a preliminary report.

Authors:  Adriane L Baylis; Benjamin Munson; Karlind T Moller
Journal:  Cleft Palate Craniofac J       Date:  2008-03

Review 9.  Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.

Authors:  Ann Swillen; Edward Moss; Sasja Duijff
Journal:  Am J Med Genet A       Date:  2018-04-25       Impact factor: 2.802

10.  22q and two: 22q11.2 deletion syndrome and coexisting conditions.

Authors:  Jennifer L Cohen; Terrence B Crowley; Daniel E McGinn; Carey McDougall; Marta Unolt; Michele P Lambert; Beverly S Emanuel; Elaine H Zackai; Donna M McDonald-McGinn
Journal:  Am J Med Genet A       Date:  2018-09-23       Impact factor: 2.802

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