Fragile X syndrome

Biol Psychiatry. 1990 Jan 15;27(2):223-40. doi: 10.1016/0006-3223(90)90652-i.

Abstract

Fragile X syndrome is the most important X-linked etiology of mental retardation and developmental disability currently known. Accumulating evidence also indicates that male and female carriers of the fragile X genetic abnormality demonstrate a relatively specific pattern of psychiatric disturbance. Fragile X males frequently manifest behaviors from the autistic spectrum whereas females show dysfunction in social interaction, thought processes, and affective regulation. In this review, an overview of the fragile X syndrome is presented with a focus on the occurrence of particular neuropsychiatric characteristics in males and females. Relevant data from recent genetic and neurobiological research is also described. The ability to study individuals with a specific genetic cause of psychopathology such as fragile X syndrome makes this condition of particular interest to biological psychiatry.

Publication types

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

MeSH terms

  • Autistic Disorder / diagnosis
  • Autistic Disorder / genetics
  • Cerebellar Cortex / pathology
  • Cerebellar Diseases / diagnosis
  • Cerebellar Diseases / genetics
  • Chromosome Fragility*
  • Female
  • Fragile X Syndrome / genetics*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mental Status Schedule
  • Pedigree
  • Phenotype
  • Sex Chromosome Aberrations / genetics*
  • Sex Factors