Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. Molecular genetic study

Br J Psychiatry. 2003 Nov:183:409-13. doi: 10.1192/bjp.183.5.409.

Abstract

Background: Velo-cardio-facial syndrome (VCFS) is associated with interstitial deletions of chromosome 22q11. About 30% of patients with VCFS have psychosis, and the rate of these deletions in schizophrenia has been reported to be about 1%. Even higher rates of VCFS deletions have been reported for childhood-onset schizophrenia.

Aims: To test the hypothesis that there is an increased rate of VCFS among patients with early-onset psychosis (age at onset <18 years). We screened 192 early-onset patients and 329 patients with adult-onset schizophrenia.

Method: We genotyped the patients and 444 healthy controls for hemizygosity of five microsatellite markers and one single nucleotide polymorphism that map to the 22q11-deleted region.

Results: One patient had a VCFS deletion, confirmed with semi-quantitative polymerase chain reaction. None of the controls showed a pattern of genotypes consistent with hemizygosity.

Conclusions: VCFS may be less frequent among patients with psychosis than previously suggested; this rate is not increased among early-onset patients.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Adult
  • Age of Onset
  • Base Sequence
  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Cleft Palate / genetics
  • Face / abnormalities*
  • Female
  • Genotype
  • Heart Defects, Congenital / genetics*
  • Homozygote
  • Humans
  • In Situ Hybridization, Fluorescence / methods
  • Male
  • Microsatellite Repeats / genetics
  • Polymerase Chain Reaction / methods
  • Polymorphism, Single Nucleotide / genetics
  • Schizophrenia / genetics*
  • Syndrome