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OthersAcquired thrombophilia |
About thrombosis Factor V Leiden Factor V Leiden is by far the most common congenital thrombophilia. In the UK it is present in 1 in 20 individuals of European origin. It is rare in people of black or Asian origin. Factor V Leiden is caused by a change in the gene for Factor V, which helps the blood to clot. To stop a clot spreading a natural blood thinner, known as Protein C, breaks down factor V. If someone has Factor V Leiden, the factor V molecule in the blood is more resistant to being broken down and the clotting process goes on for longer. This makes individuals with this condition more prone to blood clots, leading to venous thrombosis. The risk of venous thrombosis is about eight times greater in individuals with Factor V Leiden than for those without it. However Factor V Leiden does not increase the risk of arterial thrombosis, so there is no increased risk of heart attacks or strokes. Inheritance A double dose is known as homozygous Factor V Leiden. It affects 1 in 1600 people of European origin. Factor V Leiden and venous thrombosis The risk of having a venous thrombosis
is about eight times greater for an individual with heterozygous Factor
V Leiden. However this risk is relatively low and most individuals with the
condition are not affected. The risk of venous thrombosis is much higher for individuals with homozygous Factor V Leiden. It is about 80 times greater than for those without the condition. Preventing venous thrombosis
Individuals with Factor V Leiden should also seek medical advice before major surgery, or when they are likely to be immobile for a long period, as this increases the risk of venous thrombosis. Women with Factor V Leiden should seek medical advice before taking oral contraception or hormone replacement therapy, and when pregnant or planning to become pregnant. Factor V Leiden and pregnancy |
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© Lifeblood: The Thrombosis Charity 2003-2006. A
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