Preimplantation genetic diagnosis: applications for molecular medicine

Trends Mol Med. 2001 Jan;7(1):23-30. doi: 10.1016/s1471-4914(00)01867-0.

Abstract

Preimplantation genetic diagnosis is an alternative to prenatal diagnosis for the detection of genetic disorders. Tests are conducted on single cells biopsied from embryos before they are implanted, allowing the selection of unaffected embryos before a pregnancy has been established. Thus, the issue of pregnancy termination is circumvented. The use of preimplantation genetic diagnosis might have a significant impact on in vitro fertilization success rates as well as allowing the diagnosis of inherited disease.

Publication types

  • Review

MeSH terms

  • Abortion, Spontaneous / genetics
  • Chromosome Aberrations / epidemiology
  • Chromosome Aberrations / genetics
  • Chromosome Disorders
  • DNA Mutational Analysis
  • Embryo Transfer
  • Ethics, Medical
  • Female
  • Fertilization in Vitro
  • Forecasting
  • Genetic Diseases, Inborn / diagnosis*
  • Genetic Diseases, Inborn / embryology
  • Genetic Diseases, Inborn / prevention & control
  • Humans
  • In Situ Hybridization, Fluorescence
  • Micromanipulation
  • Mosaicism
  • Polymerase Chain Reaction
  • Pregnancy
  • Pregnancy Outcome
  • Preimplantation Diagnosis* / methods
  • Reproductive Techniques / legislation & jurisprudence