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
Polysaccharide storage myopathy is a muscle disease that can cause "tying up" symptoms: muscle weakness, shivers, work intolerance, and even muscle wasting particularly in the hindquarters.
Unlike the other inherited disorders that we test for, PSSM1 is not recessive. This means that horses which inherit the PSSM1 mutation from just one parent can show signs of this disorder. To complicate matters, not all horses with the PSSM1 mutation show signs of this disease - its effects range all the way from negligible to fatal. Not all cases of tying up are caused by PSSM1 either: one study found that only 65% of a group of horses with moderate to severe signs carried this particular mutation.
Testing for PSSM1 is valuable for both breeders and riders in eliminating or confirming a major known cause of tying up. Speak to your veterinarian about the management of PSSM1 horses.
PSSM1 has been found in:
It may also occur in other breeds and crosses.