Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series-Reference-Cited by-同舟云学术

Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series

Published:2018-05-19 Issue:10 Volume:176 Page:2146-2159
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Butcher Nancy J.¹²^ORCID,Boot Erik³⁴^ORCID,Lang Anthony E.⁵⁶,Andrade Danielle⁶⁷,Vorstman Jacob⁸,McDonald-McGinn Donna²⁹¹⁰,Bassett Anne S.¹³¹¹¹²^ORCID

Affiliation:

1. Clinical Genetics Research Program; Centre for Addiction and Mental Health; Toronto, Ontario Canada

2. The 22q and You Center, Children's Hospital of Philadelphia; Philadelphia Pennsylvania

3. The Dalglish Family 22q Clinic for Adults with 22q11.2 Deletion Syndrome; University Health Network; Toronto Ontario Canada

4. De Hartekamp Groep; Centre for People with Intellectual Disability; Haarlem The Netherlands

5. Morton and Gloria Shulman Movement Disorders Centre and Krembil Research Institute; Toronto Western Hospital and the Edmond J. Safra Program in Parkinson's Disease Research, University of Toronto; Toronto Ontario Canada

6. Division of Neurology, Department of Medicine; University of Toronto; Toronto Ontario Canada

7. Division of Neurology, Epilepsy Genetics Program; Toronto Western Hospital and Krembil Neuroscience Centre, University of Toronto; Toronto Ontario Canada

8. Department of Psychiatry, Brain Center Rudolf Magnus; University Medical Center Utrecht; Utrecht The Netherlands

9. Clinical Genetics Centre and Section of Genetic Counseling, The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

10. Department of Pediatrics, The Perelman School of Medicine; University of Pennsylvania; Philadelphia Pennsylvania

11. Department of Psychiatry, and Campbell Family Mental Health Research Institute; University of Toronto; Toronto Ontario Canada

12. Department of Mental Health, and Division of Cardiology; Department of Medicine, and Toronto General Research Institute, University Health Network; Toronto Ontario Canada

Funder

Canadian Institutes of Health Research

National Institute of Mental Health

University of Toronto McLaughlin Centre (ASB)

Dalglish Fellowship in 22q11.2 deletion syndrome (EB)

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38708/fullpdf

Reference104 articles.

1. The schizophrenia phenotype in 22q11 deletion syndrome;Bassett;The American Journal of Psychiatry,2003

2. Premature death in adults with 22q11.2 deletion syndrome;Bassett;Journal of Medical Genetics,2009

3. Clinical features of 78 adults with 22q11 deletion syndrome;Bassett;American Journal of Medical Genetics Part A,2005

4. Neuropsychiatric aspects of 22q11.2 deletion syndrome: Considerations in the prenatal setting;Bassett;Prenatal Diagnosis,2017

5. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;Journal of Pediatrics,2011

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