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There are two main types of haemophilia Bleeding into deep tissues or joints usually develops within hours of trauma. Haemophilia a, which occurs due to low amounts of clotting factor viii, and haemophilia b, which occurs due to low levels of clotting factor ix

Hemophilia occurs when a clotting factor is missing or levels of the clotting factor are low The extent of factor deficiency determines the probability and severity of bleeding Hemophilia is usually inherited, meaning a person is born with the disorder (congenital)

Congenital hemophilia is classified by the type of clotting factor that's low.

In hemophilia, you don’t have enough clotting factors to prevent uncontrollable bleeding Hemophilia is a rare blood disorder that keeps your blood from clotting If you have hemophilia, a minor injury may cause you to bleed a lot Hemophilia is a genetic disorder where blood doesn’t clot properly

Mild cases may show excessive bleeding only after trauma, while severe cases may involve frequent nosebleeds, bruising, and. Hemophilia is an inherited disorder It prevents blood from clotting properly People with hemophilia bleed longer than usual

This bleeding can range from mild to severe

In severe cases, people with hemophilia can bleed to death. Hemophilia, which means love (philia) of blood (hemo), is the most common severe hereditary hemorrhagic disorder Both hemophilia a and b result from factor viii and factor ix protein deficiency or dysfunction, respectively, and are characterized by prolonged and excessive bleeding after minor trauma or sometimes even spontaneously. Hemophilias are common hereditary bleeding disorders caused by deficiencies of either clotting factor viii or ix

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