Von-Willebrand-Disease Type 1

Order number: GSD370
€53.90

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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... more
Product information "Von-Willebrand-Disease Type 1"
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.
In the lexicon you will find more information and explanations about the article more
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Classification:
Species: Dog
Type: DNA tests
Class: Inherited diseases
Breeding clubs: Dobermann-Verein e.V.
Breed: Airedale, Akita inu, Deutscher Schäferhund, Dobermann, Golden Retriever, Mischling Hund, Sonstige, unbekannt, verschiedene Rassen
Group: Blood
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Centronuclear Myopathy (CNM)
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