Genetic Test
The VWF (Von Willebrand Factor) gene encodes a protein that plays a vital role in blood clotting.
This protein facilitates platelet adhesion at sites of vascular injury and assists in the transport of various clotting proteins within the bloodstream.
Mutations in the VWF gene are associated with Type 2 Von Willebrand Disease, a bleeding disorder characterized by qualitative defects in von Willebrand factor function.
This genetic test targets a specific mutation linked to Type 2 Von Willebrand Disease.
Disease Description
Von Willebrand disease is the most common inherited bleeding disorder in dogs.
Affected dogs may experience prolonged bleeding following surgical procedures.
While some dogs show no obvious external signs, spontaneous bleeding can frequently occur from the mouth, nose, vagina, or bladder.
Additionally, stress often acts as a trigger or precursor to bleeding episodes.
