MYH1 Myopathy / Immune-mediated Myositis (IMM)
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MYH1 Myopathy is a hereditary disease with incomplete/semi-dominant inheritance, caused by a mutation (chr11:52993878T>C; E321G) in the MYH1 Myosin Heavy Chain 1 gene. This mutation is a major risk factor horse horses to develop Immune mediated myopathy (IMM) and non-exertional rhabdomyolysis. IMM affected animals can exhibit muscle extreme loss (especially in the hind quarters), muscle... more
Product information "MYH1 Myopathy / Immune-mediated Myositis (IMM)"
MYH1 Myopathy is a hereditary disease with incomplete/semi-dominant inheritance, caused by a mutation (chr11:52993878T>C; E321G) in the MYH1 Myosin Heavy Chain 1 gene. This mutation is a major risk factor horse horses to develop Immune mediated myopathy (IMM) and non-exertional rhabdomyolysis. IMM affected animals can exhibit muscle extreme loss (especially in the hind quarters), muscle stiffness, and overall weakness. Horses with episodes of non-exertional rhabdomyolysis exhibit muscle damage (with or without atrophy) causing muscle stiffness and cramping, dark urine, and high muscle enzyme levels in the blood.
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Classification:
Type: | DNA tests |
Class: | Inherited diseases |
Species: | Horse |
Breed: | American Paint Horse, Appaloosa, Araberpinto, Australisches Stockhorse, Azteke, Baschkire, keine Angabe zur Rasse | Pferd, Mischling - Diverse Rassen | Pferd, Mustang, ONC, Paint Horse, Pinto, Pony of the Americas, Quarab, Quarter Horse, Quarter Pony, Suffield Mustang |
Group: | Musculature |
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