Unexplained fetal loss: the fetal side of thrombophilia
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.
Key Words: IUFD, thrombophilia, placenta, MTHFR, PAI-1, factor V, factor H
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A.L.T. has nothing to disclose. F.S. has nothing to disclose. S.R.G. has nothing to disclose. M.C. has nothing to disclose. L.N. has nothing to disclose. S.L. has nothing to disclose. M.E. has nothing to disclose.
PII: S0015-0282(09)03802-3
doi:10.1016/j.fertnstert.2009.09.052
© 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

