Premature ovarian failure: a phenotypic expression of fragile X premutation

S D Med. 2008 Jan;61(1):13, 15.

Abstract

Fragile X syndrome is the most common cause of mental retardation in the male. Historically, fragile X premutation was considered to be phenotypically silent. In recent reports the premutation has been associated with premature ovarian failure and fragile X-associated tremor/ataxia syndrome. This case describes a 24-year-old woman who presented with irregular menstrual cycles secondary to premature ovarian failure. Subsequent genetic analysis confirmed that she has a premutation for fragile X with 70 CGG trinucleotide repeats.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • DNA / genetics*
  • Female
  • Fragile X Mental Retardation Protein / genetics*
  • Fragile X Syndrome / complications
  • Fragile X Syndrome / genetics*
  • Humans
  • Menstrual Cycle
  • Mutation*
  • Phenotype
  • Pregnancy
  • Primary Ovarian Insufficiency / genetics*
  • Trinucleotide Repeats / genetics*

Substances

  • FMR1 protein, human
  • Fragile X Mental Retardation Protein
  • DNA