Genetic Test
The F8 (Coagulation Factor VIII) gene encodes coagulation factor VIII, which plays a crucial role in the blood clotting cascade by activating coagulation factor X.
Mutations in this gene cause factor VIII deficiency, also known as hemophilia A, a common X-linked inherited bleeding disorder.
This genetic test targets four specific mutations in the F8 gene associated with factor VIII deficiency.
Disease Description
Factor VIII deficiency is a hereditary bleeding disorder caused by impaired blood clotting due to a deficiency of coagulation factor VIII.
This condition is commonly known as hemophilia A.
Affected animals may experience prolonged bleeding at sites of trauma, the umbilical cord after birth, and spontaneous bleeding from the nose, mouth, eyes, and other areas.
