
Hemophilia A is caused my a change in the F8 gene and Hemophilia B is caused by a mutation in the F9 gene. A is the classic one while B is known as christmas disease. A form of B is known as hemophilia B Leyden and that causes excessive bleeding in adulthood but gets better after puberty. Hem
ophila C is the rarest and takes much longer to clot.

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The symptoms are simply bleeding. They may not be noticed until later in life during surgery or after trauma. Diagnostics and Detection are normally after a severe bleeding episode.
People can be treated by receiving the clotting factor by intravenous infusions which is through a vein.
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Hemophilia is more common in men. 1 in 400 to 1 in 5000 males are born with Hemophilia A and 1 in 20,000 are born with Hemophilia B worldwide. it affects all ethnic groups.
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Life expectancy isnt really affected but some may bleed to death and internal bleeding may cause problems.
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