Packages
5 panel, 6 panel (QH, Paint etc.)
Various breeds
Overo lethal white syndrome (frame overo)
Congenital stationary night blindness (appaloosa)
Polysaccharide storage myopathy type 1 (PSSM1)
Arabians, pure and part-bred
Severe combined immune deficiency (SCID)
Friesians, pure and part-bred
Warmbloods, pure and part-bred
Fell Ponies, Dale Ponies and Gypsy horses, pure and part-bred
Foal immunodeficiency syndrome (FIS)
Quarter horses and related breeds, pure and part-bred
Hyperkalemic periodic paralysis (HYPP)
Glycogen enzyme branching deficiency (GBED)
Hereditary equine regional dermal asthenia (HERDA)
Saddlebred and related breeds, pure and part-bred
Junctional epidermolysis bullosa (JEB)
Akhal Teke, pure and part-bred
Connemara, pure and part-bred
Hoof wall separation disease (HWSD)
Coat colour tests
Parentage
Us
Junctional epidermolysis bullosa (JEB) causes a failure in the skin's normal attachment to the body. Affected foals are usually born alive, but will develop sores and skin tears extremely easily. There is currently no effective treatment for JEB.
JEB is an autosomal recessive disorder. Autosomal disorders are equally likely to affect male or female horses, while "recessive" means that a horse needs to inherit the JEB mutation from both its sire and its dam to be affected. Horses that have inherited the JEB mutation from just one parent are called JEB carriers, and do not have physical signs of this disorder.
Any JEB carrier can potentially produce a foal suffering from JEB. Fortunately this is easily avoided: you simply need to ensure that the prospective foal cannot inherit the JEB mutation from both its sire and its dam. Therefore, if you have a JEB carrier horse and it is mated to a JEB-clear horse there is no risk of the foal being affected with JEB.
The Saddlebred form of JEB has been detected in Saddlebreds and Racking Horses. It may also be present in other related breeds, and part-bred horses with some Saddlebred blood.
This test is not useful for detecting JEB in heavy horses.