Von Willebrand disease
Rune, Christian and William.
Von Willebrand disease is a coagulation defect, which is located on the chromosome 12. The disease can be inherited as autosomal dominant and autosomal recessive. A carrier of severe Von Willebrand disease will not be able to create a crust of wound. A carrier of mild Von Willebrand disease will have a hard time creating crust of wounds and will for instance have frequent nosebleeds.
On this hereditary we can see that the disease is not Gender-chromosome linked. If both the parents have the mild condition there will be a 25 percent risk that they will make a child with the severe condition. The parents will have a 25 percent chance of making a child without the disease.
On this hereditary we can see that the disease is not Gender-chromosome linked. If both the parents have the mild condition there will be a 25 percent risk that they will make a child with the severe condition. The parents will have a 25 percent chance of making a child without the disease.