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Product number: GSD370

Von-Willebrand-Disease Type 1

Regular price:

€53.90

incl. VAT

Description

Genes examined

  • vWF
Application:
- Identification of heterozygous carriers
- Differential diagnosis of coagulation disorders
Von Willebrand disease (vWD) type 1 is due to a reduction of the blood clotting factor of the same name, caused by a mutation in exon 43. The mode of inheritance is autosomal recessive, only dogs with two defective genes are affected. The effect manifests itself in varying intensity depending on the need for clotting factor.
Genetics Knowledge Lexicon
Properties
Species: Dog
Category: Inherited diseases
Effect: Blood
Race: Airedale Terrier, Akita, Doberman Pincher, English Setter, German Shepherd Dog, Golden Retriever, Mixed-Breed Dog, Other, Various Dog Breeds, no breed declaration | dog
Type: DNA Tests