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Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
Wolfe, Kate; McQuillin, Andrew; Alesi, Viola; Boudry Labis, Elise; Cutajar, Peter; Dallapiccola, Bruno; Dentici, Maria Lisa; Dieux-Coeslier, Anne; Duban-Bedu, Benedicte; Duelund Hjortshøj, Tina; Goel, Himanshu; Loddo, Sara; Morrogh, Deborah; Mosca-Boidron, Anne-Laure; Novelli, Antonio; Olivier-Faivre, Laurence; Parker, Jennifer; Parker, Michael J; Patch, Christine; Pelling, Anna L; Smol, Thomas; Tümer, Zeynep; Vanakker, Olivier; van Haeringen, Arie; Vanlerberghe, Clémence; Strydom, Andre; Skuse, David; Bass, Nick.
Afiliação
  • Wolfe K; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.
  • McQuillin A; Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, United Kingdom.
  • Alesi V; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Boudry Labis E; Institut de génétique médicale, CHU Lille, Lille, France.
  • Cutajar P; Nottinghamshire Healthcare NHS Foundation Trust, Nottingham, United Kingdom.
  • Dallapiccola B; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Dentici ML; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Dieux-Coeslier A; Service de génétique clinique, CHU Lille, Lille, France.
  • Duban-Bedu B; EA7364, RADEME, Université de Lille, Lille, France.
  • Duelund Hjortshøj T; Centre de génétique chromosomique, Hopital Saint-Vincent de Paul, Lille, France.
  • Goel H; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Loddo S; Hunter Genetics, Waratah, New South Wales, Australia.
  • Morrogh D; University of Newcastle, Callaghan, New South Wales, Australia.
  • Mosca-Boidron AL; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Novelli A; North East Thames Regional Genetics Service Laboratory, London, United Kingdom.
  • Olivier-Faivre L; Service de Cytogénétique, Plateau technique de Biologie, CHU Dijon, France.
  • Parker J; Medical Genetics Unit, Medical Genetics Laboratory, Bambino Gesù Pediatric Hospital, IRCCS, Rome, Italy.
  • Parker MJ; Centre de référence Anomalies du développement et Syndromes malformatifs, FHU TRANSLAD, CHU Dijon, France.
  • Patch C; North East Thames Regional Genetics Service Laboratory, London, United Kingdom.
  • Pelling AL; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Western Bank, Sheffield, United Kingdom.
  • Smol T; King's College London, Florence Nightingale Faculty of Nursing and Midwifery, London, United Kingdom.
  • Tümer Z; Genomics England, Dawson Hall, Charterhouse Square, London, United Kingdom.
  • Vanakker O; Information Officer, Unique - The Rare Chromosome Disorder Support Group (www.rarechromo.org), The Stables, Station Road West, Oxted, Surrey, United Kingdom.
  • van Haeringen A; Institut de génétique médicale, CHU Lille, Lille, France.
  • Vanlerberghe C; EA7364, RADEME, Université de Lille, Lille, France.
  • Strydom A; Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Skuse D; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Bass N; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Am J Med Genet B Neuropsychiatr Genet ; 177(4): 397-405, 2018 06.
Article em En | MEDLINE | ID: mdl-29603867
Recurrent deletions and duplications at the 2q13 locus have been associated with developmental delay (DD) and dysmorphisms. We aimed to undertake detailed clinical characterization of individuals with 2q13 copy number variations (CNVs), with a focus on behavioral and psychiatric phenotypes. Participants were recruited via the Unique chromosomal disorder support group, U.K. National Health Service Regional Genetics Centres, and the DatabasE of genomiC varIation and Phenotype in Humans using Ensembl Resources (DECIPHER) database. A review of published 2q13 patient case reports was undertaken to enable combined phenotypic analysis. We present a new case series of 2q13 CNV carriers (21 deletion, 4 duplication) and the largest ever combined analysis with data from published studies, making a total of 54 deletion and 23 duplication carriers. DD/intellectual disabilities was identified in the majority of carriers (79% deletion, 70% duplication), although in the new cases 52% had an IQ in the borderline or normal range. Despite the median age of the new cases being only 9 years, 64% had a clinical psychiatric diagnosis. Combined analysis found attention deficit hyperactivity disorder (ADHD) to be the most frequent diagnosis (48% deletion, 60% duplication), followed by autism spectrum disorders (33% deletion, 17% duplication). Aggressive (33%) and self-injurious behaviors (33%) were also identified in the new cases. CNVs at 2q13 are typically associated with DD with mildly impaired intelligence, and a high rate of childhood psychiatric diagnoses-particularly ADHD. We have further characterized the clinical phenotype related to imbalances of the 2q13 region and identified it as a region of interest for the neurobiological investigation of ADHD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 2 / Deficiências do Desenvolvimento / Transtornos Mentais Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 2 / Deficiências do Desenvolvimento / Transtornos Mentais Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido