Von Willebrand’s Disease Type I (VWD1) Test | GenSol Diagnostics
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Von Willebrand’s Disease Type I (VWD1)

$40.00

Von Willebrand disease (vWD) is a genetic disorder that prevents normal blood clotting and can cause extended bleeding following injury. The disorder results from a deficiency or lack of sufficient von Willebrand factor (vWf) which functions as a binding protein during blood clotting. Three types of vWD have been identified in dogs to date and are known as vWD type 1, 2 and 3. Within these three types there are five different genetic mutations that are currently known that lead to canine vWD.

Von Willebrand’s disease type 1 (VWD1) results in reduction in normal levels of vWf to approximately 5-10% of normal. Since some vWf is produced in dogs homozygous for the VWD1 mutation, this form of the disorder is considered to be less serious than type 2 and 3. The mutation (G>A substitution) has variable penetrance and is recessive requiring two copies of the mutation in affected dogs. Typical symptoms of the disease encompass excessive or abnormal bleeding following injury or the presence of blood in various bodily secretions (urine, feces, etc.).

Bernese Mountain Dog
Coton de Tulear
Doberman Pinscher
Drentse Patrijshond
German Pinscher
Goldendoodle
Kerry Blue Terrier
Labradoodle
Manchester Terrier
Papillion
Pembroke Welsh Corgi
Poodle
Stabyhoun

A (CLEAR/NORMAL): These dogs have two copies of the normal gene and will neither develop von Willebrand’s Disease Type I disease nor pass this mutation to their offspring.

B (CARRIER/NOT AFFECTED): These dogs have one copy of the normal gene and one copy of the mutation associated with this disease. They will not develop von Willebrand’s Disease Type I disease but will, if bred, pass the mutation to 50% of its offspring, on average.

C (AT RISK/AFFECTED): These dogs have two copies of the mutation associated with this disease and are susceptible to develop problems with blood clotting.

Von Willebrand’s Disease Type I (VWD1)

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