4.1 Article

Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2-p12.1 and two large chromosomal abnormalities at 16q22.3-q24.3 and Xq23-q28

Journal

CLINICAL CASE REPORTS
Volume 3, Issue 4, Pages 201-207

Publisher

WILEY
DOI: 10.1002/ccr3.192

Keywords

Childhood-onset schizophrenia; copy number variant; cytogenetic; partial monsomy X; partial trisomy 16

Funding

  1. NIMH [MH080128, MH68380, MH31593, MH40856, MH43271]
  2. NARSAD Grant
  3. NIH

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Childhood-onset schizophrenia is rare, comprising 1% of known schizophrenia cases. Here, we report a patient with childhood-onset schizophrenia who has three large chromosomal abnormalities: an inherited 2.2 Mb deletion of chromosome 3p12.2-p12.1, a de novo 16.7 Mb duplication of 16q22.3-24.3, and a de novo 43 Mb deletion of Xq23-q28.

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