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J Med Genet 43:887-892 doi:10.1136/jmg.2006.043380
  • Letters to JMG

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia

  1. J L Seal1,
  2. M C Gornick1,
  3. N Gogtay1,
  4. P Shaw1,
  5. D K Greenstein1,
  6. M Coffey1,
  7. P A Gochman1,
  8. T Stromberg1,
  9. Z Chen2,
  10. B Merriman2,
  11. S F Nelson2,
  12. J Brooks3,
  13. S Arepalli3,
  14. F Wavrant-De Vrièze3,
  15. J Hardy3,
  16. J L Rapoport1,
  17. A M Addington1
  1. 1Child Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA
  2. 2Department of Human Genetics, UCLA School of Medicine, UCLA, Los Angeles, California, USA
  3. 3Laboratory of Neurogenetics, NIA, National Institutes of Health
  1. Correspondence to:
 A M Addington
 10 Center Drive, Building 10, Room 3N202, Bethesda, MD 20892, USA;addingta{at}mail.nih.gov
  • Received 13 April 2006
  • Accepted 4 May 2006
  • Revised 2 May 2006
  • Published Online First 8 June 2006

Abstract

Schizophrenia is a severe mental disorder affecting approximately 1% of the world’s population. Although the aetiology of schizophrenia is complex and multifactorial, with estimated heritabilities as high as 80%, genetic factors are the most compelling. Childhood-onset schizophrenia (COS), defined as onset of schizophrenia before the age of 13 years, is a rare and malignant form of the illness that may have more salient genetic influence. The first known case of paternal segmental uniparental isodisomy (iUPD) on 5q32-qter in a patient with COS is described, which adds to the previously known high rates of chromosomal abnormalities reported in this sample. iUPD is a rare genetic condition in which the offspring receives two chromosomal homologues from one parent. Segmental UPD is defined as UPD on a portion of a chromosome with biparental inheritance seen in the rest of the homologous pair. Complications owing to this abnormality may arise from malfunctioning imprinted genes or homozygosity of recessive disease-causing mutations. This aberration became apparent during whole-genomic screening of a COS cohort and is of particular interest because 5q has been implicated in schizophrenia by several genomewide linkage studies and positive gene associations. This report, therefore, presents more evidence that schizophrenia susceptibility gene, or genes, may be found on distal 5q.

Footnotes

  • Published Online First 8 June 2006

  • Competing interests: None declared.