Literature DB >> 24985125

Array-CGH in children with mild intellectual disability: a population-based study.

Charles Coutton1, Klaus Dieterich, Véronique Satre, Gaëlle Vieville, Florence Amblard, Marie David, Christine Cans, Pierre-Simon Jouk, Francoise Devillard.   

Abstract

UNLABELLED: Intellectual disability (ID) is characterized by limitation in intellectual function and adaptive behavior, with onset in childhood. Frequent identifiable causes of ID originate from chromosomal imbalances. During the last years, array-CGH has successfully contributed to improve the diagnostic detection rate of genetic abnormalities in patients with ID. Most array-CGH studies focused on patients with moderate or severe intellectual disability. Studies on genetic etiology in children with mild intellectual disability (ID) are very rare. We performed array-CGH analysis in 66 children with mild intellectual disability assessed in a population-based study and for whom no genetic etiology was identified. We found one or more copy number variations (CNVs) in 20 out of 66 (~30 %) patients with a mild ID. In eight of them (~12 %), the CNVs were certainly responsible for the phenotype and in six they were potentially pathogenic for ID. Altogether, array-CGH helped to determine the etiology of ID in 14 patients (~21 %).
CONCLUSION: Our results underscore the clinical relevance of array-CGH to investigate the etiology of isolated idiopathic mild ID in patients or associated with even subtle dysmorphic features or congenital malformations.

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Year:  2014        PMID: 24985125     DOI: 10.1007/s00431-014-2367-6

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  38 in total

Review 1.  Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation.

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Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

4.  American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

Authors:  Hutton M Kearney; Erik C Thorland; Kerry K Brown; Fabiola Quintero-Rivera; Sarah T South
Journal:  Genet Med       Date:  2011-07       Impact factor: 8.822

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6.  Epidemiology of mental retardation--a Swedish survey.

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Journal:  Brain Dev       Date:  1983       Impact factor: 1.961

7.  The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.

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Journal:  J Med Genet       Date:  2007-03-16       Impact factor: 6.318

8.  Development of a multiplex ligation-dependent probe amplification (MLPA) assay for quantification of the OCRL1 gene.

Authors:  Charles Coutton; Nicole Monnier; John Rendu; Joël Lunardi
Journal:  Clin Biochem       Date:  2010-01-04       Impact factor: 3.281

9.  Phenotypic heterogeneity of genomic disorders and rare copy-number variants.

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Journal:  N Engl J Med       Date:  2012-09-12       Impact factor: 91.245

Review 10.  Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.

Authors:  Gurdeep S Sagoo; Adam S Butterworth; Simon Sanderson; Charles Shaw-Smith; Julian P T Higgins; Hilary Burton
Journal:  Genet Med       Date:  2009-03       Impact factor: 8.822

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  7 in total

1.  22q13 Microduplication Syndrome in Siblings with Mild Clinical Phenotype: Broadening the Clinical and Behavioral Spectrum.

Authors:  Anikó Ujfalusi; Orsolya Nagy; Beáta Bessenyei; Györgyi Lente; Irén Kántor; Ádám J Borbély; Katalin Szakszon
Journal:  Mol Syndromol       Date:  2020-04-04

2.  A Single-Nucleotide Polymorphism in the Promoter of Porcine ARHGAP24 Gene Regulates Aggressive Behavior of Weaned Pigs After Mixing by Affecting the Binding of Transcription Factor p53.

Authors:  Qinglei Xu; Jing Zhao; Yanli Guo; Mingzheng Liu; Allan P Schinckel; Bo Zhou
Journal:  Front Cell Dev Biol       Date:  2022-04-01

3.  Copy number variants prioritization after array-CGH analysis - a cohort of 1000 patients.

Authors:  Isabel Marques Carreira; Susana Isabel Ferreira; Eunice Matoso; Luís Miguel Pires; José Ferrão; Ana Jardim; Alexandra Mascarenhas; Marta Pinto; Nuno Lavoura; Cláudia Pais; Patrícia Paiva; Lúcia Simões; Francisco Caramelo; Lina Ramos; Margarida Venâncio; Fabiana Ramos; Ana Beleza; Joaquim Sá; Jorge Saraiva; Joana Barbosa de Melo
Journal:  Mol Cytogenet       Date:  2015-12-30       Impact factor: 2.009

4.  Optimized Generation of Functional Neutrophils and Macrophages from Patient-Specific Induced Pluripotent Stem Cells: Ex Vivo Models of X(0)-Linked, AR22(0)- and AR47(0)- Chronic Granulomatous Diseases.

Authors:  Julie Brault; Erwan Goutagny; Narasimha Telugu; Kaifeng Shao; Mathurin Baquié; Véronique Satre; Charles Coutton; Didier Grunwald; Jean-Paul Brion; Vincent Barlogis; Jean-Louis Stephan; Dominique Plantaz; Jürgen Hescheler; Karl-Heinz Krause; Tomo Sarić; Marie José Stasia
Journal:  Biores Open Access       Date:  2014-12-01

5.  Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.

Authors:  Miriam Kessi; Juan Xiong; Liwen Wu; Lifen Yang; Fang He; Chen Chen; Nan Pang; Haolin Duan; Wen Zhang; Ahmed Arafat; Fei Yin; Jing Peng
Journal:  Front Neurol       Date:  2018-11-19       Impact factor: 4.003

6.  Microarray testing in clinical diagnosis: an analysis of 5,300 New Zealand patients.

Authors:  Adrian Mc Cormack; Karen Claxton; Fern Ashton; Philip Asquith; Edward Atack; Roberto Mazzaschi; Paula Moverley; Rachel O'Connor; Methat Qorri; Karen Sheath; Donald R Love; Alice M George
Journal:  Mol Cytogenet       Date:  2016-03-31       Impact factor: 2.009

7.  Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report.

Authors:  Alina Bogliş; Adriana S Cosma; Florin Tripon; Claudia Bãnescu
Journal:  Medicine (Baltimore)       Date:  2020-08-14       Impact factor: 1.817

  7 in total

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