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

  • Rudd D
  • Axelsen M
  • Epping E
  • et al.
N/ACitations
Citations of this article
15Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

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.

Cite

CITATION STYLE

APA

Rudd, D., Axelsen, M., Epping, E. A., Andreasen, N., & Wassink, T. (2015). 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. Clinical Case Reports, 3(4), 201–207. https://doi.org/10.1002/ccr3.192

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free