Analyze Diet
Equine veterinary journal2010; 42(2); 170-173; doi: 10.2746/042516409X479595

Dysautonomia in a six-year-old mule in the United States.

Abstract: Equine dysautonomia, also known as equine grass sickness (EGS), is a well documented disease in several countries. To the authors' knowledge, EGS has not been reported previously in North America. This report describes EGS in a 6-year-old female mule in the USA. Failure initially to consider EGS resulted in a delayed diagnosis. EGS should be considered as a differential diagnosis and appropriate diagnostic tests performed in similar cases in North America.
Publication Date: 2010-02-17 PubMed ID: 20156255DOI: 10.2746/042516409X479595Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Case Reports
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research presents the first documented case of equine grass sickness (EGS), also known as equine dysautonomia, in North America. By revealing a delayed diagnosis of EGS in a young mule, the study emphasizes the need for considering EGS in corresponding situations in North America.

Introduction to Equine Grass Sickness

  • Equine grass sickness (EGS), or equine dysautonomia, is a disease typically found in horses that primarily affects the nervous system of the digestive tract.
  • This disease has been well-documented and reported in several countries, but until now, has not been identified in North America.

The Case Study: A 6-year-old Mule

  • The research article centers around a 6-year-old female mule in the USA showing symptoms of equine grass sickness.
  • Initial attempts at diagnosing the illness failed to identify EGS, causing a delay in the correct diagnosis and inappropriate treatment.

Significance of the Research

  • The importance of this study lies in its identification of EGS in a North American case for the first time.
  • The report underlines the necessity to consider EGS as a potential diagnosis when encountering similar clinical presentations in North American equines.

Future Implications

  • This study translates to practical implications for the approach to sick equines in North America, especially in cases where standard diagnoses do not seem to match the symptoms.
  • Going forward, the presence of EGS in North America should not be overlooked, and appropriate diagnostic tests ought to be carried out to identify it accurately and promptly for effective treatment.

Cite This Article

APA
Wright A, Beard L, Bawa B, Bras J. (2010). Dysautonomia in a six-year-old mule in the United States. Equine Vet J, 42(2), 170-173. https://doi.org/10.2746/042516409X479595

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 42
Issue: 2
Pages: 170-173

Researcher Affiliations

Wright, A
  • Department of Clinical Sciences and Department of Diagnostic Medicine/Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA.
Beard, L
    Bawa, B
      Bras, J

        MeSH Terms

        • Animals
        • Equidae
        • Fatal Outcome
        • Female
        • Primary Dysautonomias / diagnosis
        • Primary Dysautonomias / epidemiology
        • Primary Dysautonomias / veterinary
        • United States / epidemiology

        Citations

        This article has been cited 2 times.
        1. Laus F, Corsalini J, Mandara MT, Bazzano M, Bertoletti A, Gialletti R. Equine grass sickness in italy: a case series study.. BMC Vet Res 2021 Aug 6;17(1):264.
          doi: 10.1186/s12917-021-02966-ypubmed: 34362361google scholar: lookup
        2. Husulak ML, Lohmann KL, Gabadage K, Wojnarowicz C, Marqués FJ. Equine motor neuron disease in 2 horses from Saskatchewan.. Can Vet J 2016 Jul;57(7):771-6.
          pubmed: 27429468