The fragile X premutation: into the phenotypic fold

Curr Opin Genet Dev. 2002 Jun;12(3):278-83. doi: 10.1016/s0959-437x(02)00299-x.

Abstract

Premutation alleles (55-200 CGG repeats) of the fragile X mental retardation 1 gene (FMR1) are known to contribute to the fragile X phenotype through genetic instability and transmission of full mutation alleles (>200 repeats). There is now mounting evidence that the premutation alleles themselves contribute to clinical involvement, including premature ovarian failure among female carriers and a new tremor/ataxia syndrome among older male carriers. Recent observations also provide direct evidence of dysregulation of the FMR1 gene in the premutation range, which may explain many of the clinical observations.

Publication types

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

MeSH terms

  • Female
  • Fragile X Mental Retardation Protein
  • Fragile X Syndrome / epidemiology
  • Fragile X Syndrome / genetics*
  • Humans
  • Mutation*
  • Nerve Tissue Proteins / genetics*
  • Prevalence
  • Primary Ovarian Insufficiency / genetics
  • RNA-Binding Proteins*

Substances

  • FMR1 protein, human
  • Nerve Tissue Proteins
  • RNA-Binding Proteins
  • Fragile X Mental Retardation Protein