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Tierarztliche Praxis1997; 25(3); 241-243;

[Equine motor neuron disease (EMND). A case report].

Abstract: A 13-year-old warmblood mare was presented because of progressive weight loss, general weakness and trembling. On examination the horse stood with its head lowered and the limbs placed under the body. On lifting its head spasms of the neck muscles could be observed. At the same time the horse developed trembling over the lower neck and muscle fasciculations continued over the whole body. Additional signs included frequent recumbency, polyphagia and facial hyperaesthesia. The horse showed no signs of ataxia. Haematology was normal. Blood biochemistry revealed slight increased aspartate aminotransferase (AST: 1060 U/I) and creatine kinase levels (CK: 441 U/I). Based on the clinical findings equine motor neuron disease was diagnosed. The horse was euthanatized due to poor prognosis and the progression of symptoms. The typical neurodegenerative changes found on histological examination of the spinal cord confirmed the diagnosis.
Publication Date: 1997-05-01 PubMed ID: 9289883
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Summary

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The research article discusses a case study of a 13-year-old mare who was diagnosed with the equine motor neuron disease (EMND), characterized by progressive weight loss, general weakness, and trembling among other symptoms. The mare was eventually euthanized due to its deteriorating condition, and subsequent examination of its spinal cord confirmed the EMND diagnosis.

Case Presentation

  • The article begins by presenting the case of a 13-year-old warmblood mare that exhibited symptoms of progressive weight loss, general weakness, and trembling.
  • The horse stood with its head lowered, kept its limbs under its body, and experienced neck muscle spasms when its head was lifted. This led to trembling in its lower neck and ongoing muscle twitching across its entire body.

Additional Symptoms and Medical Examination

  • In addition to the initial symptoms, the horse was frequently recumbent, displayed excessive hunger and increased sensitivity in the face. However, it didn’t show any signs of loss of muscle coordination or balance (ataxia).
  • A haematology test of the horse showed normal results, implying the absence of any general blood disorders or infections.
  • However, blood biochemistry showed slightly increased aspartate aminotransferase (AST) and creatine kinase (CK) levels, which indicate muscle damage or diseases.

Diagnosis and Euthanization

  • Based on the symptoms and the results of the biochemical analysis, the horse was diagnosed with equine motor neuron disease (EMND), a degenerative condition affecting motor neurons leading to muscle weakness and atrophy.
  • Due to poor prognosis and worsening of symptoms, the horse was euthanatized.

Post-Mortem Examination

  • After euthanization, a histological examination of the horse’s spinal cord was undertaken.
  • The examination revealed typical neurodegenerative changes, which further confirmed the EMND diagnosis.

Cite This Article

APA
Landolt G, Feige K, Grest P. (1997). [Equine motor neuron disease (EMND). A case report]. Tierarztl Prax, 25(3), 241-243.

Publication

ISSN: 0303-6286
NlmUniqueID: 7501042
Country: Germany
Language: ger
Volume: 25
Issue: 3
Pages: 241-243

Researcher Affiliations

Landolt, G
  • Klinik für Wiederkäuer- und Pferdemedizin, Universität Zürich.
Feige, K
    Grest, P

      MeSH Terms

      • Animals
      • Aspartate Aminotransferases / blood
      • Clinical Enzyme Tests
      • Creatine Kinase / blood
      • Female
      • Horse Diseases
      • Horses
      • Motor Neuron Disease / diagnosis
      • Motor Neuron Disease / physiopathology
      • Motor Neuron Disease / veterinary
      • Muscle, Skeletal / physiopathology
      • Neurons / pathology
      • Posture
      • Spinal Cord / pathology

      Citations

      This article has been cited 1 times.
      1. Cappai MG, Dimauro C, Biggio GP, Cherchi R, Accioni F, Pudda F, Boatto G, Pinna W. The metabolic profile of Asinara (albino) and Sardo donkeys (pigmented) (Equus asinus L., 1758) points to unequivocal breed assignment of individuals. PeerJ 2020;8:e9297.
        doi: 10.7717/peerj.9297pubmed: 32714654google scholar: lookup