Literature DB >> 29307037

Autism Spectrum Symptomatology Among Children with Duplication 7q11.23 Syndrome.

Bonita P Klein-Tasman1, Carolyn B Mervis2.   

Abstract

Gold-standard diagnostic assessments of autism spectrum disorder (ASD) symptomatology were conducted on 63 children (mean CA: 8.81 years) with 7q11.23 duplication syndrome, one of the copy number variants identified by Sanders et al. (Neuron 70:863-885, 2011a) as associated with ASD. ASD classification rate was 39.6% for the Autism Diagnostic Interview-Revised and 25.4% for the Autism Diagnostic Observation Schedule-2 (ADOS-2). Based on these assessments combined with clinical judgment, 19.0% of children were diagnosed with ASD. Reasons for these discrepancies are discussed, as are differences in rate of diagnosis as a function of sex, age, and ADOS-2 module administered and differences in intellectual and adaptive behavior abilities as a function of presence or absence of ASD diagnosis and ADOS-2 module administered. Implications are addressed.

Entities:  

Keywords:  7q11.23 duplication syndrome; Autism spectrum disorders; Selective mutism; Social anxiety

Mesh:

Year:  2018        PMID: 29307037      PMCID: PMC6003247          DOI: 10.1007/s10803-017-3439-z

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


  41 in total

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Review 4.  Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.

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Journal:  Brain Res       Date:  2010-12-01       Impact factor: 3.252

5.  Rare de novo and transmitted copy-number variation in autistic spectrum disorders.

Authors:  Dan Levy; Michael Ronemus; Boris Yamrom; Yoon-ha Lee; Anthony Leotta; Jude Kendall; Steven Marks; B Lakshmi; Deepa Pai; Kenny Ye; Andreas Buja; Abba Krieger; Seungtai Yoon; Jennifer Troge; Linda Rodgers; Ivan Iossifov; Michael Wigler
Journal:  Neuron       Date:  2011-06-09       Impact factor: 17.173

6.  Diagnostic yield of chromosomal microarray analysis in an autism primary care practice: which guidelines to implement?

Authors:  Susan G McGrew; Brittany R Peters; Julie A Crittendon; Jeremy Veenstra-Vanderweele
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7.  Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.

Authors:  Emma Strong; Darci T Butcher; Rajat Singhania; Carolyn B Mervis; Colleen A Morris; Daniel De Carvalho; Rosanna Weksberg; Lucy R Osborne
Journal:  Am J Hum Genet       Date:  2015-07-09       Impact factor: 11.025

8.  Severe impairments of social interaction and associated abnormalities in children: epidemiology and classification.

Authors:  L Wing; J Gould
Journal:  J Autism Dev Disord       Date:  1979-03

9.  A Two-Hit Model of Autism: Adolescence as the Second Hit.

Authors:  Giorgia Picci; K Suzanne Scherf
Journal:  Clin Psychol Sci       Date:  2014-08-04

Review 10.  Explaining differences in age at autism spectrum disorder diagnosis: a critical review.

Authors:  Amy M Daniels; David S Mandell
Journal:  Autism       Date:  2013-06-20
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  11 in total

1.  Autism Spectrum Symptomatology in Children with Williams Syndrome Who Have Phrase Speech or Fluent Language.

Authors:  Bonita P Klein-Tasman; Faye van der Fluit; Carolyn B Mervis
Journal:  J Autism Dev Disord       Date:  2018-09

2.  Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models.

Authors:  Nathan Kopp; Katherine McCullough; Susan E Maloney; Joseph D Dougherty
Journal:  Hum Mol Genet       Date:  2019-10-15       Impact factor: 6.150

3.  The Behavioral Phenotype of 7q11.23 Duplication Syndrome Includes Risk for Oppositional Behavior and Aggression.

Authors:  Bonita P Klein-Tasman; Brianna D Yund; Carolyn B Mervis
Journal:  J Dev Behav Pediatr       Date:  2022-05-17       Impact factor: 2.988

Review 4.  A cross-comparison of cognitive ability across 8 genomic disorders.

Authors:  Michael Mortillo; Jennifer G Mulle
Journal:  Curr Opin Genet Dev       Date:  2021-05-31       Impact factor: 4.665

5.  Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.

Authors:  Christine M Freitag; Andreas G Chiocchetti; Afsheen Yousaf; Regina Waltes; Denise Haslinger; Sabine M Klauck; Eftichia Duketis; Michael Sachse; Anette Voran; Monica Biscaldi; Martin Schulte-Rüther; Sven Cichon; Markus Nöthen; Jörg Ackermann; Ina Koch
Journal:  Transl Psychiatry       Date:  2020-07-05       Impact factor: 6.222

6.  Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.

Authors:  Rebecca M Pollak; Melissa M Murphy; Michael P Epstein; Michael E Zwick; Cheryl Klaiman; Celine A Saulnier; Jennifer G Mulle
Journal:  Mol Autism       Date:  2019-07-16       Impact factor: 7.509

7.  7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling.

Authors:  Maria Lisa Dentici; Paola Bergonzini; Francesco Scibelli; Cristina Caciolo; Paola De Rose; Francesca Cumbo; Viola Alesi; Rossella Capolino; Ginevra Zanni; Lorenzo Sinibaldi; Antonio Novelli; Marco Tartaglia; Maria Cristina Digilio; Bruno Dallapiccola; Stefano Vicari; Paolo Alfieri
Journal:  Brain Sci       Date:  2020-11-11

8.  Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.

Authors:  Farah Qaiser; Yue Yin; Carolyn B Mervis; Colleen A Morris; Bonita P Klein-Tasman; Elaine Tam; Lucy R Osborne; Ryan K C Yuen
Journal:  Orphanet J Rare Dis       Date:  2021-01-06       Impact factor: 4.123

Review 9.  Williams syndrome.

Authors:  Beth A Kozel; Boaz Barak; Chong Ae Kim; Carolyn B Mervis; Lucy R Osborne; Melanie Porter; Barbara R Pober
Journal:  Nat Rev Dis Primers       Date:  2021-06-17       Impact factor: 65.038

10.  Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.

Authors:  Nathan D Kopp; Phoebe C R Parrish; Michael Lugo; Joseph D Dougherty; Beth A Kozel
Journal:  Mol Genet Genomic Med       Date:  2018-07-15       Impact factor: 2.183

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