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Musculoskeletal System
Myopathies in Ruminants and Pigs
Genetic Myopathies in Ruminants and Pigs
Caprine Myotonia
Phosphorylase Deficiency in Charolais Cattle
Porcine Malignant Hyperthermia
Porcine RN (–) Glycogen Storage Disease
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Sections in Veterinary Professionals
  • Behavior
  • Circulatory System
  • Clinical Pathology and Procedures
  • Digestive System
  • Emergency Medicine and Critical Care
  • Endocrine System
  • Exotic and Laboratory Animals
  • Eye and Ear
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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 Ruminants and Pigs
  • Infectious Myopathies in Ruminants and Pigs
  • Nutritional Myopathies in Ruminants and Pigs
  • Toxic Myopathies in Ruminants and Pigs
  • Traumatic Myopathies in Cattle
  • Genetic Myopathies in Ruminants and Pigs
     
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    Genetic Myopathies in Ruminants and Pigs

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    Caprine Myotonia

    Myotonia congenita in goats is due to an autosomal dominant mutation in the skeletal muscle chloride channel that has incomplete penetrance. Goats with this mutation have been selected for as a breed and are commonly referred to as “fainting goats.” Clinical signs ranging from stiffness after rest to marked general rigidity after visual, tactile, or auditory stimulation usually develop by 6 wk of age. These signs remain throughout the animal's life but are not progressive. A diagnosis of myotonia is made by identifying the characteristic “dive bomber” discharges in electromyography and/or by genetic testing.

    Phosphorylase Deficiency in Charolais Cattle

    A mutation in the myophosphorylase gene in Charolais cattle produces signs of exercise intolerance and muscle necrosis very similar to nutritional myodegeneration. The disease has now been recognized in many countries including the USA and New Zealand. Animals become exercise intolerant may collapse when forced to exercise and develop muscle necrosis characterized by elevated serum CK and prolonged recumbency. Supportive care during episodes has allowed many young animals to survive and unknowingly enter the breeding herd.

    Porcine Malignant Hyperthermia

    Malignant hyperthermia in swine (see Malignant Hyperthermia) is due to an autosomal recessive genetic mutation in the skeletal muscle ryanodine receptor 1gene (RYR1) that causes abnormal meat quality in swine. Pietrain, Poland China, and certain strains of Landrace pigs are affected. During transportation or anesthesia, pigs develop elevated body temperature, extreme rigidity of the skeletal muscles, and lactic acidosis. At slaughter affected muscles become pale, soft, exudative muscle, which diminishes meat quality. A genetic test is available to diagnose affected and carrier animals.

    Porcine RN (–) Glycogen Storage Disease

    The RN(−) (rendement Napole) phenotype is common in Hampshire pigs. It is due to an autosomal dominant mutation in the protein kinase AMP-activated gamma 3 subunit gene (PRKAG3), which encodes the gamma 3 isoform of AMP-activated protein kinase (AMPK). Clinically pigs appear normal; however, the 70% increase in glycogen content in skeletal muscle causes poor meat quality at slaughter.

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

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