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Von Willebrand (VWF) is a blood protein that binds with plasma and aids in clotting, deficiency or dysfunctioning of Von Willebrand factor causes Von Willebrand disease. It is an inherited hematological disorder in which blood is unable to clot. There are three types of Von Willebrand disease:
It is a genetic disorder, mostly the gene is inherited from the parents, characterized by deficiency or non functional Von Willebrand factor, a clotting factor. In rare cases it is due to gene mutation. If it is acquired it cannot be passed on from the affected individual to the offspring.
Risk factors of Von Willebrand Disease include:
Many people show symptoms of other minor bleeding disorders, therefore making it difficult to differentiate from vWd.
Your doctor may take a detailed history and do relevant examinations.
Following tests are done to reach the diagnosis:
The aim of the treatment is to increase the Von Willebrand factor and decrease bleeding.
The following are used in the medication:
Visit your doctor if you are experiencing prolonged bleeding which is difficult to stop.
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Dear Customer! We only allow given quantity of the selected product. If you want to order a greater quantity, please fill this form so that our sales team can get in touch with you to facilitate your order
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