Schizophrenia in an adult with 6p25 deletion syndrome

Am J Med Genet A. 2006 Jun 1;140(11):1208-13. doi: 10.1002/ajmg.a.31222.

Abstract

Chromosomal deletions at 6p25-p24 are rare findings in patients with developmental delay. There is limited information about the adult phenotype. We present a 36-year-old patient with schizophrenia, mild mental retardation, progressive hearing deficits, and characteristic facial features. Ocular (Axenfeld-Rieger anomaly) abnormalities were diagnosed in infancy; vision, however, has remained unimpaired. There were no other major congenital anomalies. Brain imaging showed only minor changes. There was no family history of intellectual deficits or psychosis. Karyotyping revealed a 6p25 deletion, and detailed fluorescence in situ hybridization (FISH) analyses using 23 probes confirmed a 6.7 Mb 6p25-pter deletion. The breakpoint is near a possible 6p25-p24 locus for schizophrenia. Psychotic illness may be part of the neurodevelopmental abnormalities and long-term outcome of patients with 6p terminal deletions. Other similarly affected patients likely remain to be diagnosed in adult populations of schizophrenia and/or mental retardation.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Adult
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 6 / genetics*
  • Eye Abnormalities
  • Female
  • Hearing Disorders / pathology
  • Humans
  • In Situ Hybridization, Fluorescence
  • Intellectual Disability / pathology
  • Karyotyping
  • Phenotype
  • Schizophrenia / pathology*
  • Syndrome

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