Optimising management in Turner syndrome: from infancy to adult transfer

Arch Dis Child. 2006 Jun;91(6):513-20. doi: 10.1136/adc.2003.035907.

Abstract

Turner syndrome can be defined as loss or abnormality of the second X chromosome in at least one cell line in a phenotypic female. The condition occurs in approximately 1 in every 2000 live female births,(1) so that in the UK the prevalence for any year of life is in the region of 200 girls. The condition is much more common in utero, it being estimated that 1-2% of all conceptuses are affected, of whom only 1% will survive to term.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Estrogens / therapeutic use
  • Ethinyl Estradiol / therapeutic use
  • Female
  • Genotype
  • Growth Hormone / therapeutic use
  • Humans
  • Infant
  • Phenotype
  • Turner Syndrome / complications
  • Turner Syndrome / genetics
  • Turner Syndrome / therapy*

Substances

  • Estrogens
  • Ethinyl Estradiol
  • Growth Hormone