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The veterinary quarterly2005; 27(2); 65-75; doi: 10.1080/01652176.2005.9695187

Hereditary skeletal muscle diseases in the horse. A review.

Abstract: Since riders nowadays are expecting the highest level of performance from their horses, muscular disorders therefore represent a major problem for the equine athlete. A lot of research has been done to identify muscular disorders and their etiopathogenesis. Both acquired and inherited forms of muscle diseases have been described. In this review only the latter forms will be mentioned. Major signs of all muscle disorders are muscular stiffness, cramping or pain, muscular fasciculations, muscular atrophy and exercise intolerance. Muscle biopsies can help to identify the cause of rhabdomyolysis or muscular atrophy. However, especially in hereditary muscular diseases, a lot of questions are still to be answered. Increasing knowledge of the etiopathogenesis and newer diagnostic tests may lead to a more accurate diagnosis of the individual diseases in future.
Publication Date: 2005-07-19 PubMed ID: 16022342DOI: 10.1080/01652176.2005.9695187Google Scholar: Lookup
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Summary

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The research article focuses on the genetic diseases affecting the skeletal muscles of horses and its impact on their athletic performance. It discusses the symptoms, diagnosis, and future prospects in relation to understanding and diagnosing these conditions.

Hereditary Muscular Diseases in Horses

  • The researchers in this paper discuss the increasing demands placed on performance horses and how muscular disorders, particularly those of a hereditary nature, could significantly impact athletic performance and quality of life for these animals.
  • The focus of this research is on hereditary muscle diseases, which suggest a genetic cause much like in humans. They mention the key indicators of these disorders which include muscular stiffness, cramping or pain, muscle twitches (fasciculations), muscle wastage (atrophy), and intolerance to exercise.

Symptoms and Initial Diagnosis

  • The researchers highlight muscular stiffness, cramping, pain, fasciculations, atrophy, and exercise intolerance as common, often noticeable signs of muscle disorders in horses.
  • In order to identify the root cause of these symptoms, especially when they result in rhabdomyolysis (rapid muscle breakdown) or muscular atrophy, muscle biopsies can be beneficial. These involve taking a small sample of muscle tissue for examination and offers insight into the type and extent of muscle damage.

Unanswered Questions and Future Prospects

  • The authors state that, despite advancements in knowledge and understanding, there are still many unanswered questions regarding hereditary muscular disorders in horses.
  • They hold promising views for the future, stating that an increase in knowledge about the underlying causes and development (etiology and pathogenesis) of these disorders, together with advances in diagnostic tests, could lead to more accurate and reliable diagnoses. This future development may help to better manage and treat these conditions, improving the quality of life and performance of affected horses.

Cite This Article

APA
Nollet H, Deprez P. (2005). Hereditary skeletal muscle diseases in the horse. A review. Vet Q, 27(2), 65-75. https://doi.org/10.1080/01652176.2005.9695187

Publication

ISSN: 0165-2176
NlmUniqueID: 7909485
Country: England
Language: English
Volume: 27
Issue: 2
Pages: 65-75

Researcher Affiliations

Nollet, H
  • Department of Large Animal Internal Medicine, Faculty of Veterinary Medicine, University of Ghent, Merelbeke, Belgium. Heidi.Nollet@UGent.be
Deprez, P

    MeSH Terms

    • Animals
    • Glycogen Storage Disease / physiopathology
    • Glycogen Storage Disease / veterinary
    • Horse Diseases / genetics
    • Horse Diseases / physiopathology
    • Horses
    • Mitochondrial Myopathies / physiopathology
    • Mitochondrial Myopathies / veterinary
    • Muscular Diseases / genetics
    • Muscular Diseases / physiopathology
    • Muscular Diseases / veterinary
    • Myotonia Congenita / physiopathology
    • Myotonia Congenita / veterinary
    • Paralysis, Hyperkalemic Periodic / physiopathology
    • Paralysis, Hyperkalemic Periodic / veterinary
    • Rhabdomyolysis / physiopathology
    • Rhabdomyolysis / veterinary

    References

    This article includes 89 references

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