Literature DB >> 21689796

Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.

Brian H Y Chung1, Irene Drmic, Christian R Marshall, Daria Grafodatskaya, Melissa Carter, Bridget A Fernandez, Rosanna Weksberg, Wendy Roberts, Stephen W Scherer.   

Abstract

Dup(X)(p11.22-p11.23) has been shown to be associated with intellectual disability (ID, also referred to as mental retardation). Here, we characterize a 4.64 Mb de novo duplication of the same Xp11.22-p11.23 ID region in a female, but for this reference case the diagnosis was Autism Spectrum Disorder (ASD). Besides ASD, she also had very persistent trichotillomania, anxiety symptoms and some non-specific dysmorphic features. We report the detailed clinical features, as well as refine the rearrangement breakpoints of this disease-associated copy number variation region, which encompasses more than 50 genes. We propose that in addition to ID, the phenotypic spectrum associated with dup(X)(p11.22-p11.23) can include ASD, language impairment, and/or other primary psychiatric disorders.
Copyright © 2011 Elsevier Masson SAS. All rights reserved.

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Year:  2011        PMID: 21689796     DOI: 10.1016/j.ejmg.2011.05.008

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  8 in total

1.  Protein kinase WNK3 regulates the neuronal splicing factor Fox-1.

Authors:  A-Young Lee; Wei Chen; Steve Stippec; Jon Self; Fan Yang; Xiaojun Ding; She Chen; Yu-Chi Juang; Melanie H Cobb
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-01       Impact factor: 11.205

Review 2.  Male gender bias in autism and pediatric autoimmunity.

Authors:  Kevin G Becker
Journal:  Autism Res       Date:  2012-03-17       Impact factor: 5.216

3.  GRASP1 Regulates Synaptic Plasticity and Learning through Endosomal Recycling of AMPA Receptors.

Authors:  Shu-Ling Chiu; Graham Hugh Diering; Bing Ye; Kogo Takamiya; Chih-Ming Chen; Yuwu Jiang; Tejasvi Niranjan; Charles E Schwartz; Tao Wang; Richard L Huganir
Journal:  Neuron       Date:  2017-03-09       Impact factor: 17.173

4.  A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical Spectrum.

Authors:  Pinar Arican; Dilek Cavusoglu; Pinar Gencpinar; Berk Ozyilmaz; Taha Resid Ozdemir; Nihal Olgac Dundar
Journal:  J Pediatr Genet       Date:  2017-12-18

Review 5.  Glutamatergic candidate genes in autism spectrum disorder: an overview.

Authors:  Andreas G Chiocchetti; Hanna S Bour; Christine M Freitag
Journal:  J Neural Transm (Vienna)       Date:  2014-02-04       Impact factor: 3.575

6.  Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes.

Authors:  Tejasvi S Niranjan; Cindy Skinner; Melanie May; Tychele Turner; Rebecca Rose; Roger Stevenson; Charles E Schwartz; Tao Wang
Journal:  PLoS One       Date:  2015-02-13       Impact factor: 3.240

7.  Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability.

Authors:  Christina Grau; Molly Starkovich; Mahshid S Azamian; Fan Xia; Sau Wai Cheung; Patricia Evans; Alex Henderson; Seema R Lalani; Daryl A Scott
Journal:  PLoS One       Date:  2017-04-17       Impact factor: 3.240

8.  Xp11.2 Duplication in Females: Unique Features of a Rare Copy Number Variation.

Authors:  Márta Czakó; Ágnes Till; Judith Zima; Anna Zsigmond; András Szabó; Anita Maász; Béla Melegh; Kinga Hadzsiev
Journal:  Front Genet       Date:  2021-04-14       Impact factor: 4.599

  8 in total

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