von Willebrand disease type 2 (vWD2)

LABOKLIN Service ID: 8014

The most common form of canine hereditary bleeding disorders is the von Willebrand disease (vWD). The condition is caused by a quantitative or qualitative deficiency of von Willebrand factor (vWF), which is an essential component of the blood coagulation cascade. A defect of the vWF leads to uncontrolled bleeding upon inquiries or spontaneous. Clinical symptoms of vWD are highly heterogeneous from mild bleeding to severe life-threatening blood loss and may be aggravated by mental or physical stress. Typical signs are: repeated gastrointestinal bleeding with or without diarrhea, epistaxis, bleeding after dental extraction, gingival bleeding, ecchymosis, extended bleeding during heat, lameness due to bleeding inside the joints, excessive bleeding upon nail cutting or postoperative. VWD is divided into three major categories: type 1, type 2 and type 3 as well as diverse subtypes. The clinical expression of canine vWD type 2 is generally severe. This kind of bleeding variant is rare in dogs occurring only in German Shorthaired Pointers and German Wirehaired Pointers.

Method	TaqMan SNP assay
Breed list	German Short-haired Pointing Dog, German Wire-haired Pointing Dog
Heredity	autosomal recessive
Duration	3 - 5 days after arrival of the sample in the lab