Topic Overview
What is von Willebrand's disease?
Von Willebrand's disease is a bleeding disorder in which a protein
in your body's blood system is missing or does not work well. The protein is
called von Willebrand factor. If the von Willebrand factor is working properly,
it helps your blood clot. Clotting stops the bleeding when you are cut or
injured.
The von Willebrand factor usually carries another blood-clotting
protein called factor VIII. If you have von Willebrand's disease, the two
proteins may not attach properly to each other. Your blood will not clot as
well as it should.
There are three major types of the disease:1
- Type 1: A shortage of von
Willebrand factor (mild). This type of von Willebrand's disease can
result in mild to moderate bleeding episodes, depending on how much von
Willebrand factor is missing. Between 70% to 80% of all cases of von
Willebrand's disease are type 1.2 Some people with
type 1 disease do not need treatment and may not be aware that they have a
blood disorder.
- Type 2: A flawed von Willebrand
factor (usually mild). Although the body produces normal amounts of the
von Willebrand factor, it doesn't work properly. Type 2 is further classified
(such as 2a or 2b) depending on the type of flaw.
- Type 3: A complete lack of von Willebrand factor (more
severe). Type 3 von Willebrand's disease is very rare. When the body
does not produce von Willebrand factor, the cells (platelets)
needed to form a clot do not work properly and clotting factor VIII levels are
low, both of which can lead to severe bleeding. People with type 3 disease are
in more danger of
anemia and excessive bleeding after an accident or
during surgery.
What causes von Willebrand's disease?
Von Willebrand's disease usually is passed down through families.
It is the most common bleeding disorder present at birth (congenital)1, but most cases are mild. About 1% of people may inherit this
disease.3 If one parent has von Willebrand's disease,
a child has a 50% chance of having the condition.1 Men
and women are equally likely to have von Willebrand's disease.
What are the symptoms?
Excessive bleeding is the main symptom of von Willebrand's disease.
The severity of the condition varies from person to person, even within the
same family.1 Over half of all women with von
Willebrand's disease have very heavy menstrual bleeding. Other symptoms include
frequent nosebleeds and heavy bleeding after injury or surgery.1
Von Willebrand's disease causes symptoms similar to the bleeding
disorder
hemophilia.
How is von Willebrand's disease
diagnosed?
Von Willebrand's disease can be hard to diagnose. If you have
symptoms that suggest a blood clotting disorder, your doctor will ask about
your medical history, especially about episodes of excessive bleeding. Tests
that can help with the diagnosis include:
- Blood tests that measure bleeding time, von
Willebrand factor activity levels, or von Willebrand factor
antigen.
- Genetic testing that shows a defect in your von Willebrand
factor.
How is it treated?
If you have von Willebrand's disease, you probably will need to
prevent and treat bleeding episodes throughout your life. The course of von
Willebrand's disease is difficult to predict because it may stay at the same
level of activity or get better or worse as you get older.
Treatment may include:
- Desmopressin medicine, to help increase the
production of von Willebrand factor.
- Replacing the clotting factor
in your blood.
- Medicine that helps prevent the breakdown of blood
clots (antifibrinolytic agents).
- Hormone therapy, to control heavy
menstrual periods in women.
- Topical medicine to control bleeding
(thrombin powder).
- Avoiding medicines, such as aspirin, that can
affect bleeding.
Frequently Asked Questions
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