Hemophilia is a rare genetic disorder that affects the body's ability to form blood clots, which can lead to prolonged bleeding and difficulty in stopping bleeding after an injury or surgery. There are two main types of hemophilia: hemophilia A, which is caused by a deficiency of clotting factor VIII, and hemophilia B, which is caused by a deficiency of clotting factor IX. {Do Not Self-Medicate, Contact Your Doctor} This article is for information only and not for treatment. If you have any medical problem, consult a good doctor. If you follow these medical advices, do so at your own risk. Hemophilia is an X-linked recessive disorder, which means it is caused by a gene mutation on the X chromosome. Females have two X chromosomes, while males have one X and one Y chromosome. If a male inherits the hemophilia gene mutation on his X chromosome, he will develop the disorder because he does not have another X chromosome to compensate for the mutation. However, f...
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