Journal
CLINICAL CASE REPORTS
Volume 3, Issue 4, Pages 201-207Publisher
WILEY
DOI: 10.1002/ccr3.192
Keywords
Childhood-onset schizophrenia; copy number variant; cytogenetic; partial monsomy X; partial trisomy 16
Categories
Funding
- NIMH [MH080128, MH68380, MH31593, MH40856, MH43271]
- NARSAD Grant
- NIH
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available