Cytogenetic studies of males with schizophrenia. Screening for the fragile X chromosome and other chromosomal abnormalities

Schizophr Res. 1988 Jul-Aug;1(4):277-81. doi: 10.1016/0920-9964(88)90004-7.

Abstract

Genetic factors appear to play a role in the etiology of schizophrenia, although no specific genetic mechanism has yet been identified. As a preliminary measure in the search for the chromosomal location of a gene or genes relevant to this illness, cytogenetic screening of populations of patients might provide clues for further in depth molecular studies. Additionally, since the X chromosome has been implicated as a possible site, specific examinations aimed at identifying abnormalities in this chromosome including the presence of the fragile X site, could also be important. The following report reviews the previous literature on chromosomal aberrations in schizophrenia and presents data from a new survey of 46 unrelated male patients with schizophrenia. No chromosomal aberrations or folate-sensitive fragile sites were found in samples from these patients.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Chromosome Aberrations*
  • Chromosome Fragile Sites
  • Chromosome Fragility
  • Humans
  • Male
  • Middle Aged
  • Schizophrenia / genetics*
  • X Chromosome*