Hemophilia is usually an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery. Blood contains many proteins called clotting factors that can help to stop bleeding.
What’s the disease called when your blood doesn’t clot?
Hemophilia is a rare disorder in which your blood doesn’t clot normally because it lacks sufficient blood-clotting proteins (clotting factors). If you have hemophilia, you may bleed for a longer time after an injury than you would if your blood clotted normally.
Can you get hemophilia later in life?
The majority of hemophilia cases are genetic, affect males and are diagnosed fairly early in childhood. However, there are rare cases of hemophilia that develop later in life and are called “acquired hemophilia.”
How serious is von Willebrand disease?
Rarely, von Willebrand disease can cause uncontrollable bleeding, which can be life-threatening. Other complications of von Willebrand disease can include: Anemia. Women who have heavy menstrual bleeding can develop iron deficiency anemia.
Can hemophilia be cured?
There is currently no cure for hemophilia. Effective treatments do exist, but they are expensive and involve lifelong injections several times per week to prevent bleeding.
What vitamin deficiency causes clots?
It is essential for the formation of several substances called coagulation factors as well as protein C and protein S that work together to clot the blood when injuries to blood vessels occur and to prevent excessive clotting. Insufficient vitamin K can lead to excessive bleeding and easy bruising.
How are blood clotting disorders treated?
Your doctor may prescribe anticoagulants, or *blood thinners, before, during, and/or after surgery or medical procedures to prevent excessive blood clotting.
Is hemophilia A or B worse?
Recent evidence suggests that hemophilia B is clinically less severe than hemophilia A, highlighting the need to discuss further therapeutic options for each type of hemophilia. The study, “Haemophilia B is clinically less severe than haemophilia A: further evidence,” was published in Blood Transfusion.
What is the life expectancy for a person with hemophilia?
The median life expectancy of men with severe hemophilia (clotting factor level, <2% of normal) was 63 years, and, for those with mild or moderate hemophilia, it was 75 years, compared with 78 years for the overall British male population.
What race is most affected by hemophilia?
The average age of persons with hemophilia in the United States is 23.5 years. Compared to the distribution of race and ethnicity in the U.S. population, white race is more common, Hispanic ethnicity is equally common, while black race and Asian ancestry are less common among persons with hemophilia.
At what age is von Willebrand disease diagnosed?
76% of men with VWD had been diagnosed by age 10, but 50% of women with VWD were not diagnosed until after age 12.
Is von Willebrand disease considered a rare disease?
Platelet-type von Willebrand disease (PT-VWD), also known as pseudo-von Willebrand disease, is an extremely rare genetic disorder characterized by prolonged bleeding time.
Can you get a blood clot if you have von Willebrand disease?
If you have von Willebrand’s disease, your blood doesn’t clot well because you don’t have a certain protein in your blood or you have low levels of it. This protein is called the von Willebrand factor.
Can you have a baby if you have hemophilia?
If the mother is a hemophilia carrier, there is a chance that the baby will be born with hemophilia. In families with a known history of hemophilia, or in those with a prenatal genetic diagnosis of hemophilia, one can plan special testing for hemophilia before the baby’s delivery.
What foods to avoid if you have hemophilia?
Food and supplements to avoid
- large glasses of juice.
- soft drinks, energy drinks, and sweetened tea.
- heavy gravies and sauces.
- butter, shortening, or lard.
- full-fat dairy products.
- foods containing trans fats, including fried. foods and baked goods (pastries, pizza, pie, cookies, and crackers)
What is the best treatment for hemophilia?
The best way to treat hemophilia is to replace the missing blood clotting factor so that the blood can clot properly. This is typically done by injecting treatment products, called clotting factor concentrates, into a person’s vein.