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Musculoskeletal System
Myopathies in Horses
Overview of Myopathies in Horses
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  • Behavior
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Chapters in Musculoskeletal System
  • Musculoskeletal System Introduction
  • Congenital and Inherited Anomalies of the Musculoskeletal System
  • Dystrophies Associated with Calcium, Phosphorus, and Vitamin D
  • Arthropathies in Large Animals
  • Lameness in Cattle
  • Lameness in Goats
  • Lameness in Horses
  • Lameness in Pigs
  • Lameness in Sheep
  • Myopathies in Ruminants and Pigs
  • Myopathies in Horses
  • Bovine Secondary Recumbency
  • Lameness in Small Animals
  • Arthropathies and Related Disorders in Small Animals
  • Myopathies in Small Animals
  • Osteopathies in Small Animals
  • Sarcocystosis
Topics in Myopathies in Horses
  • Overview of Myopathies in Horses
  • Exertional Myopathies in Horses
  • Infectious Myopathies in Horses
  • Immune-Mediated Myopathies in Horses
  • Nutritional Myopathies in Horses
  • Toxic Myopathies in Horses
  • Plants Causing Myopathies in Horses
  • Traumatic and Anesthetic Myopathies in Horses
  • Muscle Cramping in Horses
  • Myotonic Disorders in Horses
  • Hereditary and Congenital Myopathies in Horses
 
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Overview of Myopathies in Horses

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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 MyopathiesTables). Genetic causes of non-exertional rhabdomyolysis include glycogen branching enzyme deficiency (foals), malignant hyperthermia (Quarter horses), and polysaccharide storage myopathy.

Table 1

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Differential Diagnoses of Equine Myopathies

Non-exercise-associated Rhabdomyolysis

Inflammatory myopathies

Clostridial myositis

Influenza myositis

Sarcocystis myositis

Immune-mediated myopathy

Nutritional myopathy

Vitamin E and selenium deficiency

Toxic myopathy

Ionophore toxicity

Pasture myopathies

Rayless goldenrod/white snakeroot

Cassia occidentalis

Atypical myoglobinuria

Traumatic myopathy

Compressive anesthetic myopathy

Trauma

Genetic myopathies

Glycogen branching enzyme deficiency in Quarter horses

Polysaccharide storage myopathy types 1 and 2

Malignant hyperthermia in Quarter horses

Exertional Rhabdomyolysis

Focal muscle strain

Sporadic tying-up (overexertion)

Chronic tying-up

Dietary imbalances, vitamins, minerals, electrolytes

Polysaccharide storage myopathy type 1 and 2

Malignant hyperthermia

Recurrent exertional rhabdomyolysis

Idiopathic chronic exertional rhabdomyolysis

Exertional Myopathy with Normal CK

Mitochondrial myopathy

Muscle Atrophy

Myogenic atrophy

Severe rhabdomyolysis

Disuse

Cushing's disease

Immune-mediated myositis (rapid atrophy)

Polysaccharide storage myopathy

Neurogenic atrophy

Equine protozoal myelitis

Local nerve trauma

Equine motor neuron disease

Muscle Fasciculations

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

Differential Diagnoses of Equine Myopathies

Non-exercise-associated Rhabdomyolysis

Inflammatory myopathies

Clostridial myositis

Influenza myositis

Sarcocystis myositis

Immune-mediated myopathy

Nutritional myopathy

Vitamin E and selenium deficiency

Toxic myopathy

Ionophore toxicity

Pasture myopathies

Rayless goldenrod/white snakeroot

Cassia occidentalis

Atypical myoglobinuria

Traumatic myopathy

Compressive anesthetic myopathy

Trauma

Genetic myopathies

Glycogen branching enzyme deficiency in Quarter horses

Polysaccharide storage myopathy types 1 and 2

Malignant hyperthermia in Quarter horses

Exertional Rhabdomyolysis

Focal muscle strain

Sporadic tying-up (overexertion)

Chronic tying-up

Dietary imbalances, vitamins, minerals, electrolytes

Polysaccharide storage myopathy type 1 and 2

Malignant hyperthermia

Recurrent exertional rhabdomyolysis

Idiopathic chronic exertional rhabdomyolysis

Exertional Myopathy with Normal CK

Mitochondrial myopathy

Muscle Atrophy

Myogenic atrophy

Severe rhabdomyolysis

Disuse

Cushing's disease

Immune-mediated myositis (rapid atrophy)

Polysaccharide storage myopathy

Neurogenic atrophy

Equine protozoal myelitis

Local nerve trauma

Equine motor neuron disease

Muscle Fasciculations

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

Last full review/revision March 2012 by Stephanie J. Valberg, DVM, PhD, DACVIM

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