22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy

Author:

Wither Robert G.1,Borlot Felippe123,MacDonald Alex4,Butcher Nancy J.45,Chow Eva W. C.46,Bassett Anne S.45678,Andrade Danielle M.13

Affiliation:

1. Division of Neurology; Department of Medicine; Toronto Western Hospital; Krembil Neuroscience Centre; University of Toronto; Toronto Ontario Canada

2. Department of Neurology; Clinical Neurosciences Center; University of Utah; Salt Lake City Utah U.S.A.

3. Krembil Neurosciences Epilepsy Genetics Program; Toronto Western Hospital; University of Toronto; Toronto Ontario Canada

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

5. Institute of Medical Science; University of Toronto; Toronto Ontario Canada

6. Department of Psychiatry; University of Toronto; Toronto Ontario Canada

7. Division of Cardiology; Department of Medicine; Dalglish Family Hearts and Minds Clinic for Adults with 22q11.2 Deletion Syndrome; Toronto General Research Institute; University Health Network; Toronto Ontario Canada

8. Department of Psychiatry; University Health Network; Toronto Ontario Canada. Campbell Family Mental Health Research Institute; Centre for Addiction and Mental Health; Toronto Ontario Canada

Funder

Brain and Behaviour Foundation Young Investigator grant

Canadian Institutes of Health Research

Canada Research Chairs

Brain Canada Mental Health Training Award

Universidade Católica de Brasília

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference33 articles.

1. Molecular and genetic aspects of DiGeorge/velocardiofacial syndrome;Driscoll;Methods Mol Med,2006

2. Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms;Guna;J Neurodev Disord,2015

3. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;J Pediatr,2011

4. Characteristics of 22q 11.2 deletion syndrome undiagnosed until adulthood: an example suggesting the importance of psychiatric manifestations;Furuya;BMJ Case Rep

5. Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome;Boot;Am J Med Genet A,2015

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