People with hemophilia are at very high risk of hemorrhage (severe, heavy, uncontrollable bleeding) from injuries such as motor vehicle accidents and also from surgery.
Hemophilia is a genetic disease, therefore people who have ancestors who were hemophiliacs have a greater chance of getting it.
*family members with hemophilia *family history of bleeding
You have to be born with hemophilia, it is not something people can "catch".
Yes of course, people with hemophilia live with it there whole lives so they learn to be very cautious.
Hemophilia itself does not directly cause death; rather, it is a genetic disorder that affects blood clotting, leading to an increased risk of bleeding. Historically, individuals with severe hemophilia faced higher mortality rates due to complications from uncontrollable bleeding or infections. Advances in treatment, such as factor replacement therapy, have significantly improved life expectancy and quality of life for those with hemophilia. However, precise statistics on deaths specifically attributed to hemophilia can vary and are not easily quantified.
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 affects approximately 1 in 10,000 people. The percentage is then approximately 0.01%.
No, hemophilia does not confer an advantage against malaria. People with sickle-cell anemia do have an immunity, of sorts.
Not all people with Hemophilia have AIDS or HIV. Due to very lax screening in blood/plasma collection centers and inadequate screening and purification on the manufacturing ends during the 1980s many hemophiliacs were infected with HIV by the medications used to treat hemophilia. Roughly 50% of the hemophilia population (or 10,000 individuals) in the United States were infected during the 1980s in this manner. Today, the number of people with hemophilia in the united states is estimated to be roughly 20,000. Approximately 2500 of the original 10,000 infected hemophilia patients are still alive. Looking at the numbers today, this means that only 12.5% of the hemophilia population has HIV and/or AIDS.
Aspirin is contraindicated in individuals with hemophilia because it inhibits platelet function, which is crucial for blood clotting. Hemophilia already impairs the body's ability to form clots due to deficiencies in clotting factors, increasing the risk of excessive bleeding. Taking aspirin can exacerbate this condition, leading to potentially life-threatening hemorrhages. Therefore, alternative pain relief options that do not affect platelet function are typically recommended for those with hemophilia.
When people would dispute who should claim the throne when the heirs died from hemophilia.
Classic hemophilia is also known as hemophilia A. It is a genetic bleeding disorder caused by a deficiency of clotting factor VIII, which is essential for normal blood coagulation. This condition leads to prolonged bleeding and increased risk of hemorrhage, particularly after injuries or surgical procedures. Hemophilia A is typically inherited in an X-linked recessive pattern, primarily affecting males.