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When this happens, the protein factors needed for normal blood
clotting are effected. In males, the single X chromosome that is effected
cannot compensate for the lack, and hence will show the defect. In females,
however, only one of the two chromosomes will be abnormal. (unless she is
unlucky enough to inherit haemophilia from both sides of the family, which is
rare.)2 The other chromosome is likely to be normal and she can therefore
compensate for this defect.
There are two types of haemophilia, haemophilia A and B. Haemophilia A is
a hereditary disorder in which bleeding is due to deficiency of the coagulation
factor VIII (VIII:C)3...
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