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Though numbers dropped, a 2008 study of the 716 Jutland horses in the Danish studbook at that time concluded that little risk of the Jutland becoming extinct existed due to inbreeding or low genetic diversity. The study, which also included populations of the Knabstrupper and Fredericksborg breeds, theorized that the greatest loss to genetic ...
It is a genetic dominant condition, though not all horses who inherit the gene will show clinical signs of being affected and the environmental triggers are not well understood at present. An estimated 7% of all Quarter Horses carry this gene. There are two forms, both linked to the same genetic variant. Affected horses may exhibit one or both ...
The Belgian Draft Horse is one breed in which JEB occurs Junctional epidermolysis bullosa ( JEB ) is an inherited disorder that is also known as red foot disease or hairless foal syndrome . [ 1 ] JEB is the result of a genetic mutation that inhibits protein production that is essential for skin adhesion. [ 2 ]
Hereditary equine regional dermal asthenia (HERDA), also known as hyperelastosis cutis (HC), is an inherited autosomal recessive connective tissue disorder. It develops from a homozygous recessive mutation that weakens collagen fibers that allow the skin of the animal to stay connected to the rest of the animal.
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Cerebellar abiotrophy (CA), also called cerebellar cortical abiotrophy (CCA), is a genetic neurological disease in animals, best known to affect certain breeds of horses, dogs and cats. It can also develop in humans.
The movement of horses at an animal welfare charity's farm has been suspended after a mare tested positive for a highly infectious respiratory disease. A recent arrival at World Horse Welfare's ...
Glycogen-branching enzyme deficiency (GBED) is an inheritable glycogen storage disease affecting American Quarter Horses and American Paint Horses. It leads to abortion, stillbirths, or early death of affected animals. The human form of the disease is known as glycogen storage disease type IV.