Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome

Author:

Fiksinski Ania M.12ORCID,Schneider Maude34,Murphy Clodagh M.56,Armando Marco37,Vicari Stefano7,Canyelles Jaume M.8,Gothelf Doron9,Eliez Stephan3,Breetvelt Elemi J.2,Arango Celso10,Vorstman Jacob A. S.11121

Affiliation:

1. Department of Psychiatry, Rudolf Magnus Institute of Neuroscience; University Medical Center Utrecht; Utrecht The Netherlands

2. Dalglish Family 22q Clinic for Adults with 22q11.2 Deletion Syndrome; Toronto General Hospital, University Health Network, and Clinical Genetics Research Program, Centre for Addiction and Mental Health; Toronto Ontario Canada

3. Developmental Imaging and Psychopathology Lab, Department of Psychiatry, School of Medicine; University of Geneva; Geneva Switzerland

4. Center for Contextual Psychiatry, Department of Neurosciences; KU Leuven; Leuven Belgium

5. Sackler Institute for Translational Neurodevelopment and Department of Forensic and Neurodevelopmental Sciences, King's College London; Institute of Psychiatry, Psychology & Neuroscience; London UK

6. Behavioural and Developmental Psychiatry Clinical Academic Group; Behavioural Genetics Clinic, Adult Autism and ADHD Service, South London and Maudsley Foundation NHS Trust; London UK

7. Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience; Children Hospital Bambino Gesù; Rome Italy

8. Hospital Universitario Fundacion Alcorcon; Alcorcon Espana

9. Child and Adolescent Psychiatry Unit Edmond and Lily Safra Children's Hospital, Sheba Medical Center; Sagol School of Neuroscience and Sackler School of Medicine Tel Aviv University; Tel Aviv Israel

10. Child and Adolescent Psychiatry Department; Hospital General Universitario Gregorio Marañón, IiSGM, School of Medicine, Universidad Complutense, CIBERSAM; Madrid Spain

11. Department of Psychiatry; The Hospital for Sick Children and University of Toronto; Toronto Ontario Canada

12. Program in Genetics and Genome Biology, Research Institute, The Hospital for Sick Children; Toronto Ontario Canada

Funder

National Institute of Mental Health

Ter Meulen Grant of the Royal Netherlands Academy of Arts and Sciences

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference90 articles.

1. Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome;Allen;Journal of Intellectual Disability Research,2014

2. A consensus statement on health care transitions for young adults with special health care needs;American Academy of Pediatrics; American Academy of Family Physicians; American College of Physicians-American Society of Internal Medicine;Pediatrics,2002

3. ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome;Antshel;Journal of the American Academy of Child and Adolescent Psychiatry,2006

4. Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: A 3-year follow-up study;Antshel;Journal of the American Academy of Child and Adolescent Psychiatry,2010

5. Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006;Autism and Developmental Disabilities Monitoring Network Surveillance Year 2006 Principal Investigators; Centers for Disease Control and Prevention (CDC);MMWR. Surveillance Summaries,2009

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