Hereditary predisposition to thrombosis due to activated protein C resistance (APCR) has been attributed to a missense mutation in the factor V gene at nucleotide 1691 (G to A), causing replacement of arginine at codon 506 with glutamine. Using an RFLP-PCR assay to detect this mutation, we measured
High prevalence of activated protein C resistance due to factor V leiden mutation in cases of intrauterine fetal death
โ Scribed by H. Rothbart; G. Ohel; J. Younis; N. Lanir; B. Brenner
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 27 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1057-0802
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โฆ Synopsis
Objective:
To test a possible association between activated protein C resistance and intrauterine fetal death. Methods: The activated protein C anticoagulant activity and factor V R506Q mutation were assessed in 14 nonpregnant women with a history of intrauterine fetal death and 14 healthy controls. Results: Four women in the study group were heterozygotes for the factor V mutation and none of the controls. The mean activated protein C activity of the study group was statistically significantly lower than that of the controls (P ฯญ 0.013).
Conclusion:
Resistance to activated protein C activity may be of etiologic importance in some cases of intrauterine fetal death.
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