Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X

Am J Med Genet. 1990 Jan;35(1):142-7. doi: 10.1002/ajmg.1320350130.

Abstract

Rett syndrome (RS) was diagnosed in a girl with a t(X;22) (p11.22;p11). This translocation was also present in her unaffected mother and her sister affected by a neurological disorder compatible with a "forme fruste" of RS. Different etiological mechanisms are considered: gene disruption, X inactivation disturbance, metabolic interference. Whatever this may be, the localization of a RS related gene to the short arm of chromosome X is likely.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Chromosomes, Human, Pair 22*
  • Female
  • Humans
  • Karyotyping
  • Phenotype
  • Rett Syndrome / diagnosis
  • Rett Syndrome / genetics*
  • Translocation, Genetic*
  • X Chromosome*