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Muscle disorders in horses present with a variety of clinical signs ranging from muscle stiffness and pain to muscle atrophy, weakness, exercise intolerance, and muscle fasciculations. The most common clinical presentation is muscle pain, stiffness, and reluctance to move due to rhabdomyolysis. Rhabdomyolysis, defined as disruption of striated skeletal muscle, can broadly be grouped into causes associated with exercise (exertional rhabdomyolysis) and causes unrelated to exercise.
Differential diagnoses for reluctance to move, acute recumbency, and discolored urine include lameness, colic, laminitis, fracture, pleuropneumonia, tetanus, aorto-iliac thrombosis, neurologic diseases resulting in recumbency or reluctance to move, intravascular hemolysis, and bilirubinuria. Causes of non-exercise-associated rhabdomyolysis include infectious (eg, Clostridium sp, influenza, Streptococcus equi, Sarcocystis) and immune-mediated myopathies, nutritional myodegeneration (vitamin E or selenium deficiency), traumatic or compressive myopathy, idiopathic pasture myopathy, and toxic muscle damage from the ingestion of ionophores (eg, monensin, lasalocid, rumensin). Plants, including white snake root and vitamin D-stimulating species, should also be considered (see Myopathies in Horses: Differential Diagnoses of Equine Myopathies ). Genetic causes of non-exertional rhabdomyolysis include glycogen branching enzyme deficiency (foals), malignant hyperthermia (Quarter horses), and polysaccharide storage myopathy.
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Table 1
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Differential Diagnoses of Equine Myopathies |
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Non-exercise-associated Rhabdomyolysis
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Inflammatory myopathies
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Nutritional myopathy
Vitamin E and selenium deficiency
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Toxic myopathy
Rayless goldenrod/white snakeroot
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Traumatic myopathy
Compressive anesthetic myopathy
Trauma
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Genetic myopathies
Glycogen branching enzyme deficiency in Quarter horses
Polysaccharide storage myopathy types 1 and 2
Malignant hyperthermia in Quarter horses
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Exertional Rhabdomyolysis
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Focal muscle strain
Sporadic tying-up (overexertion)
Chronic tying-up
Dietary imbalances, vitamins, minerals, electrolytes
Polysaccharide storage myopathy type 1 and 2
Recurrent exertional rhabdomyolysis
Idiopathic chronic exertional rhabdomyolysis
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Exertional Myopathy with Normal CK
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Mitochondrial myopathy
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Muscle Atrophy
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Myogenic atrophy
Immune-mediated myositis (rapid atrophy)
Polysaccharide storage myopathy
Neurogenic atrophy
Equine protozoal myelitis
Equine motor neuron disease
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Muscle Fasciculations
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Pain, fear
Weakness (botulism, chronic debilitation)
Electrolyte abnormalities
Equine motor neuron disease
Hyperkalemic periodic paralysis
Hypokalemia
Otobius megnini (ear tick) infestation
Myotonic dystrophy
Stiff horse syndrome
Shivers
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Last full review/revision March 2012 by Stephanie J. Valberg, DVM, PhD, DACVIM
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