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VonWillebrand 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
VonWillebrand 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 Scottish Terrier. Related variants are also found in the Shetland Sheepdog and Dutch Kooiker.
Características clínicas
La enfermedad de von Willebrand causa trastornos de la coagulación de la sangre que pueden conducir a síntomas como moretones o sangrado fácil. Estos perros a menudo corren el riesgo de sangrado excesivo durante los procedimientos veterinarios.
Información adicional
Referencias
Pubmed ID: 10668811
Omia ID: 1058