Unexplained fetal loss: the fetal side of thrombophilia

Fertil Steril. 2010 Jun;94(1):378-80. doi: 10.1016/j.fertnstert.2009.09.052. Epub 2009 Nov 11.

Abstract

Carrier status of the fetus for factor V polymorphism or double homozygosity for mutant alleles of the PAI-1 4 G/4 G and MTHFR T677 T polymorphisms must be considered risk factors for intrauterine fetal death. The clinical implications of these data need to be addressed in a prospective study to confirm our preliminary data and to answer the question of whether or not double homozygous individuals should be treated with low molecular-weight heparin and/or low-dose aspirin.

Publication types

  • Comparative Study
  • Letter

MeSH terms

  • Adult
  • Factor V / genetics
  • Female
  • Fetal Death / diagnosis
  • Fetal Death / genetics*
  • Fetal Diseases
  • Humans
  • Polymorphism, Genetic / genetics
  • Pregnancy
  • Pregnancy Complications, Hematologic / diagnosis
  • Pregnancy Complications, Hematologic / genetics*
  • Thrombophilia / diagnosis
  • Thrombophilia / genetics*

Substances

  • Factor V