Literature DB >> 16134031

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome.

Sarah E Fine1, Alison Weissman, Marsha Gerdes, Jennifer Pinto-Martin, Elaine H Zackai, Donna M McDonald-McGinn, Beverly S Emanuel.   

Abstract

In this study, we assessed the presence of autism spectrum disorders (ASD) among children with a confirmed 22q11.2 deletion (n = 98). The children's caregivers completed screening measures of ASD behaviors, and for those whose scores indicated significant levels of these behaviors, a standardized diagnostic interview (Autism Diagnostic Interview-Revised; ADI-R) was administered. Results demonstrated that over 20% of children (n = 22) were exhibiting significant levels of autism spectrum symptoms based on the screening measures. Based upon the ADI-R, 14 children qualified for a diagnosis of an ASD, and for 11 of those children a diagnosis of autism was most appropriate. These findings increase our knowledge of developmental disorders associated with the 22q11.2 deletion and point to avenues for future investigation.

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Year:  2005        PMID: 16134031      PMCID: PMC2814423          DOI: 10.1007/s10803-005-5036-9

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  42 in total

1.  Predictors of cognitive test patterns in autism families.

Authors:  S E Folstein; S L Santangelo; S E Gilman; J Piven; R Landa; J Lainhart; J Hein; M Wzorek
Journal:  J Child Psychol Psychiatry       Date:  1999-10       Impact factor: 8.982

2.  Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium.

Authors:  C M Ogilvie; J Moore; M Daker; S Palferman; Z Docherty
Journal:  Am J Med Genet       Date:  2000-02-07

3.  Prenatal and perinatal risk factors for autism.

Authors:  L Burd; R Severud; J Kerbeshian; M G Klug
Journal:  J Perinat Med       Date:  1999       Impact factor: 1.901

4.  The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.

Authors:  C Lord; S Risi; L Lambrecht; E H Cook; B L Leventhal; P C DiLavore; A Pickles; M Rutter
Journal:  J Autism Dev Disord       Date:  2000-06

5.  Autism screening questionnaire: diagnostic validity.

Authors:  S K Berument; M Rutter; C Lord; A Pickles; A Bailey
Journal:  Br J Psychiatry       Date:  1999-11       Impact factor: 9.319

Review 6.  Velo-cardio-facial syndrome: a distinctive behavioral phenotype.

Authors:  R J Shprintzen
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2000

7.  The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study.

Authors:  P Szatmari; J E MacLean; M B Jones; S E Bryson; L Zwaigenbaum; G Bartolucci; W J Mahoney; L Tuff
Journal:  J Child Psychol Psychiatry       Date:  2000-07       Impact factor: 8.982

8.  Toward a developmental operational definition of autism.

Authors:  J E Gillham; A S Carter; F R Volkmar; S S Sparrow
Journal:  J Autism Dev Disord       Date:  2000-08

9.  Genetics of childhood disorders: XLII. Autism, part 1: Diagnosis and assessment in autistic spectrum disorders.

Authors:  Catherine Lord; Fred Volkmar
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2002-09       Impact factor: 8.829

10.  Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!

Authors:  D M McDonald-McGinn; M K Tonnesen; A Laufer-Cahana; B Finucane; D A Driscoll; B S Emanuel; E H Zackai
Journal:  Genet Med       Date:  2001 Jan-Feb       Impact factor: 8.822

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  75 in total

1.  Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.

Authors:  Eleonora Napoli; Flora Tassone; Sarah Wong; Kathleen Angkustsiri; Tony J Simon; Gyu Song; Cecilia Giulivi
Journal:  J Biol Chem       Date:  2015-07-28       Impact factor: 5.157

Review 2.  A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment.

Authors:  Opal Ousley; Kimberly Rockers; Mary Lynn Dell; Karlene Coleman; Joseph F Cubells
Journal:  Curr Psychiatry Rep       Date:  2007-04       Impact factor: 5.285

Review 3.  Integrative mechanisms of oriented neuronal migration in the developing brain.

Authors:  Irina Evsyukova; Charlotte Plestant; E S Anton
Journal:  Annu Rev Cell Dev Biol       Date:  2013-08-07       Impact factor: 13.827

Review 4.  Neural phenotypes of common and rare genetic variants.

Authors:  Carrie E Bearden; David C Glahn; Agatha D Lee; Ming-Chang Chiang; Theo G M van Erp; Tyrone D Cannon; Allan L Reiss; Arthur W Toga; Paul M Thompson
Journal:  Biol Psychol       Date:  2008-02-23       Impact factor: 3.251

Review 5.  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

Review 6.  Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome.

Authors:  Matthew J Schreiner; Maria T Lazaro; Maria Jalbrzikowski; Carrie E Bearden
Journal:  Neuropharmacology       Date:  2012-10-23       Impact factor: 5.250

7.  Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome.

Authors:  Daniel W Meechan; Eric S Tucker; Thomas M Maynard; Anthony-Samuel LaMantia
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-22       Impact factor: 11.205

8.  Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?

Authors:  Kathleen Angkustsiri; Beth Goodlin-Jones; Lesley Deprey; Khyati Brahmbhatt; Susan Harris; Tony J Simon
Journal:  J Autism Dev Disord       Date:  2014-04

9.  Psychiatric disorders and autism in young children with 22q11.2 deletion syndrome compared to children with idiopathic autism.

Authors:  Yaffa Serur; Dafna Sofrin Frumer; Keren Daon; Dolly Sobol-Havia; Ronnie Weinberger; Cory Shulman; Doron Gothelf
Journal:  Eur Psychiatry       Date:  2018-11-16       Impact factor: 5.361

10.  High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

Authors:  Alexander Eckehart Urban; Jan O Korbel; Rebecca Selzer; Todd Richmond; April Hacker; George V Popescu; Joseph F Cubells; Roland Green; Beverly S Emanuel; Mark B Gerstein; Sherman M Weissman; Michael Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-14       Impact factor: 11.205

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