factor VIII deficienty
Herpes, Gonnoriha, Siffilus.
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Hemophilia is a genetic blood disorder that affects the blood's ability to clot. This results in prolonged bleeding and difficulty stopping bleeding after an injury. There are different types of hemophilia, such as hemophilia A and hemophilia B, which are caused by deficiencies of specific clotting factors.
Factor V deficiency and hemophilia are not the same; they are distinct bleeding disorders. Hemophilia primarily refers to hemophilia A, which is caused by a deficiency in factor VIII, or hemophilia B, caused by a deficiency in factor IX. Factor V deficiency, on the other hand, is a rare bleeding disorder resulting from a deficiency in factor V, which is critical for blood clotting. While both conditions lead to issues with blood coagulation, they involve different factors and have different genetic causes.
Hemophilia is a bleeding disorder that slows down the blood clotting process. People who have hemophilia often have longer bleeding after an injury or surgery. People who have severe hemophilia have spontaneous bleeding into the joints and muscles. Hemophilia occurs more commonly in males than in females.The two most common types of hemophilia are hemophilia A (also known as classic hemophilia) and hemophilia B (also known as Christmas disease). People who have hemophilia A have low levels of a blood clotting factor called factor eight (FVIII). People who have hemophilia B have low levels of factor nine (FIX).The two types of hemophilia are caused by permanent gene changes (mutations) in different genes.
Hemophilia is one disease in which blood does not clot normally. von Willebrand's Disease
There is no chance that the child will have hemophilia even if the spouse has hemophilia. Any girls the couple has will be carriers if the spouse has hemophilia.
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Can anyone be a candidate for the hemophilia a
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
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Hemophilia is not acquired from microorganisms. Hemophilia is typically a genetic disorder that can either be inherited or result from a random mutation. In rare cases non genetic forms (that can not be inherited or passed on) of hemophilia can be acquired due to liver impairment, and certain medications.