Literature DB >> 17006777

Brief report: visual-spatial deficit in a 16-year-old girl with maternally derived duplication of proximal 15q.

David Cohen1, Claire Martel, Anna Wilson, Nicole Déchambre, Céline Amy, Ludovic Duverger, Jean-Marc Guile, Eva Pipiras, Brigitte Benzacken, Hélène Cavé, Laurent Cohen, Delphine Héron, Monique Plaza.   

Abstract

Duplications of chromosome 15 may be one of the most common single genetic causes of autism spectrum disorders (ASD), aside from fragile X. Most of the cases are associated with maternally derived interstitial duplication involving 15q11-13. This case report describes a female proband with a maternally derived interstitial duplication of proximal 15q. She did not exhibit any symptoms of ASD apart from some developmental delay. By adolescence, she showed mild dysmorphism, a discrepant profile on the Wechsler Intelligence Scale for Children (Verbal IQ = 87; Performance IQ = 65) and a major deficit in visual-spatial abilities affecting fine motor skills, mathematical reasoning, visual memory and some global reading tasks. This is one of the first reports of a child with a maternal duplication who exhibits a visual-spatial deficit without ASD.

Entities:  

Mesh:

Year:  2006        PMID: 17006777     DOI: 10.1007/s10803-006-0228-5

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


  20 in total

1.  A family with a grand-maternally derived interstitial duplication of proximal 15q.

Authors:  F Z Boyar; M M Whitney; A C Lossie; B A Gray; K L Keller; H J Stalker; R T Zori; G Geffken; J Mutch; P J Edge; K S Voeller; C A Williams; D J Driscoll
Journal:  Clin Genet       Date:  2001-12       Impact factor: 4.438

Review 2.  Specific genetic disorders and autism: clinical contribution towards their identification.

Authors:  David Cohen; Nadège Pichard; Sylvie Tordjman; Clarisse Baumann; Lydie Burglen; Elsa Excoffier; Gabriela Lazar; Philippe Mazet; Clément Pinquier; Alain Verloes; Delphine Héron
Journal:  J Autism Dev Disord       Date:  2005-02

3.  Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

Authors:  F Gurrieri; A Battaglia; L Torrisi; R Tancredi; C Cavallaro; E Sangiorgi; G Neri
Journal:  Neurology       Date:  1999-05-12       Impact factor: 9.910

Review 4.  Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey.

Authors:  M Lauritsen; O Mors; P B Mortensen; H Ewald
Journal:  J Child Psychol Psychiatry       Date:  1999-03       Impact factor: 8.982

5.  Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.

Authors:  C E Browne; N R Dennis; E Maher; F L Long; J C Nicholson; J Sillibourne; J C Barber
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

6.  Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment.

Authors:  J A Thomas; J Johnson; T L Peterson Kraai; R Wilson; N Tartaglia; J LeRoux; L Beischel; L McGavran; R J Hagerman
Journal:  Am J Med Genet A       Date:  2003-06-01       Impact factor: 2.802

7.  Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.

Authors:  James S Sutcliffe; Erika L Nurmi; Paul J Lombroso
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2003-02       Impact factor: 8.829

8.  Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

Authors:  G M Repetto; L M White; P J Bader; D Johnson; J H Knoll
Journal:  Am J Med Genet       Date:  1998-09-01

9.  Autistic symptoms among children and young adults with isodicentric chromosome 15.

Authors:  S Rineer; B Finucane; E W Simon
Journal:  Am J Med Genet       Date:  1998-09-07

Review 10.  Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin.

Authors:  R Mao; S M Jalal; K Snow; V V Michels; S M Szabo; D Babovic-Vuksanovic
Journal:  Genet Med       Date:  2000 Mar-Apr       Impact factor: 8.822

View more
  5 in total

Review 1.  Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy.

Authors:  Marie Douniol; Aurélia Jacquette; Jean-Marc Guilé; Marie-Laure Tanguy; Nathalie Angeard; Delphine Héron; Monique Plaza; David Cohen
Journal:  Eur Child Adolesc Psychiatry       Date:  2009-06-19       Impact factor: 4.785

Review 2.  Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.

Authors:  Cyrille Robert; Laurent Pasquier; David Cohen; Mélanie Fradin; Roberto Canitano; Léna Damaj; Sylvie Odent; Sylvie Tordjman
Journal:  Int J Mol Sci       Date:  2017-03-12       Impact factor: 5.923

3.  Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report.

Authors:  Ji Yoon Han; Hyun Joo Lee; Young-Mock Lee; Joonhong Park
Journal:  Children (Basel)       Date:  2021-04-20

4.  Three supernumerary marker chromosomes in a patient with developmental delay, mental retardation, and dysmorphic features.

Authors:  Jie Hu; Suneeta Madan-Khetarpal; Alvaro H Serrano Russi; Sally Kochmar; Stephanie J Deward; Malini Sathanoori; Urvashi Surti
Journal:  Genet Res Int       Date:  2011-07-17

5.  The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.

Authors:  Nora Urraca; Julie Cleary; Victoria Brewer; Eniko K Pivnick; Kathryn McVicar; Ronald L Thibert; N Carolyn Schanen; Carmen Esmer; Dustin Lamport; Lawrence T Reiter
Journal:  Autism Res       Date:  2013-03-14       Impact factor: 5.216

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.