Von Willebrand Disease Type 2 (VWD2)

49.90 € inc. Vat

Acronyms: VWDII
Gene: VWF
Mutation: Point mutation
Mode of inheritance: Autosomal recessive
Breeds: Poodle, Collie Rough, Collie Smooth, German Wire- Haired Pointing Dog, German Short- Haired Pointing Dog

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Product Description

Von Willebrand disease type 2 (VWD2)

Von Willebrand disease (vWD) is a bleeding disorder of variable severity that results from a quantitative or qualitative defect in von Willebrand factor (vWF). On vascular injury, vWf mediates platelet adhesion to exposed subendothelium and is involved in platelet-to-platelet aggregation. The disease is the most common hereditary bleeding disorder and it is genetically and clinically heterogeneous. Clinical signs of the disease include spontaneous bleeding from mucosal surfaces and excess blood loss after surgery or trauma. Three clinical types, 1, 2, and 3, have been described.

Von Willebrand disease type 2 dogs have a qualitative defect in vWF, lacking high-molecular-weight multimers. Affected dogs have a severe bleeding tendency. Von Willebrand disease type 2 is inherited recessively in dogs.

Testing of affected dogs can be done by Von Willebrand disease type 2 antigen testing or by coagulation assays, but these procedures yield variable results. This variability makes it difficult for breeders to use this information to eliminate the disease-causing allele from their lines. Thus, it is highly desirable that DNA tests are run to get definitive answers.


Moser, J., Meyers, K.M., Meinkoth, J.H., and Brassard, J.A. (1996). Temporal variation and factors affecting measurement of canine von Willebrand factor. American Journal of Veterinary Research 57, 1288–1293.

Venta, P.J., Li, J., Yuzbasiyan-Gurkan, V., Brewer, G.J., and Schall, W.D. (2000). Mutation causing von Willebrand’s disease in Scottish Terriers. J. Vet. Intern. Med. 14, 10–19.