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Von Willebrand Disease (vWD) is a group of bleeding disorders caused by deficiency in the von Willebrand factor (vWF), which results in poorly functioning blood platelets and can lead to uncontrolled bleeding.
10 días laborables
Especificaciones
| Breeds | |
|---|---|
| Gene | |
| Organ | |
| specimen | Hisopo, sangre EDTA, sangre Heparina, Semen, Tejido |
| Mode of Inheritance | |
| Chromosome | |
| Also known as | |
| Year Published |
Información específica de la prueba
Von Willebrand Disease (vWD) is a group of bleeding disorders caused by deficiency in the von Willebrand factor (vWF), which results in poorly functioning blood platelets and can lead to uncontrolled bleeding. Type III (Type 3) vWD is the most severe form of the disease, and is caused by a recessive mutation to the gene vWF. This variant of Type III vWD is found in the ‘Kooikerhondje’. Related variants are also found in the Shetland Sheepdog and Scottish Terrier.
Características clínicas
Los perros afectados son susceptibles a sangrado excesivo y potencialmente mortal después de una lesión o cirugía, y pueden desarrollar sangrado espontáneo. El análisis de sangre confirmará la falta de actividad del factor von Willebrand.
Información adicional
Referencias
Pubmed ID: 9716162
Omia ID: 1058