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A 22q13.33 duplication harbouring the SHANK3 gene: does it cause neuropsychiatric disorders?
Johannessen, Maria; Haugen, Inger Breistein; Bakken, Trine Lise; Braaten, Øivind.
Affiliation
  • Johannessen M; Psychiatric Department, Oslo University Hospital, Oslo, Norway maria.johannessen@outlook.com.
  • Haugen IB; Psychiatric Department, Oslo University Hospital, Oslo, Norway.
  • Bakken TL; Psychiatric Department, Oslo University Hospital, Oslo, Norway.
  • Braaten Ø; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
BMJ Case Rep ; 12(11)2019 Nov 02.
Article in En | MEDLINE | ID: mdl-31678916
A young man with neuropsychiatric problems has a small 22q13.33 duplication. We suggest this causes his condition. His disorder may represent a 22q13.33 behavioural phenotype. In childhood, he was diagnosed with mild intellectual disability. He was later diagnosed with Tourette syndrome, atypical autism spectrum disorder and bipolar disorder. Lithium seems effective in treating his affective symptoms. He has mild dysmorphic features, full lips and protruding ears. An array comparative genomic hybridisation showed a 300 kb duplication. The duplication harbours several genes, notably SH3 and multiple ankyrin repeat domain 3 (SHANK 3). The small size helps focus on a critical region for a 22q13.33 duplication syndrome. Mutations, deletions and duplications should be kept in mind as causes of neuropsychiatric disorders, especially in a patient with dysmorphic traits.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bipolar Disorder / Tourette Syndrome / Chromosome Disorders / Autism Spectrum Disorder / Intellectual Disability Limits: Adult / Humans / Male Language: En Journal: BMJ Case Rep Year: 2019 Document type: Article Affiliation country: Norway Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bipolar Disorder / Tourette Syndrome / Chromosome Disorders / Autism Spectrum Disorder / Intellectual Disability Limits: Adult / Humans / Male Language: En Journal: BMJ Case Rep Year: 2019 Document type: Article Affiliation country: Norway Country of publication: United kingdom