Equine degenerative myeloencephalopathy.
Abstract: This article discusses the history and signalment, clinical signs, differential diagnosis, pathology, etiology and pathogenesis, and treatment and prevention of equine degenerative myeloencephalopathy.
Publication Date: 1987-08-01 PubMed ID: 3304570DOI: 10.1016/s0749-0739(17)30680-6Google Scholar: Lookup
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Summary
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This research article examines Equine Degenerative Myeloencephalopathy (EDM), a neurological disease in young horses which leads to gradual muscular dysfunction. The study looks into the causes, symptoms and possible treatment approaches, identifying Vitamin E deficiency and genetic factors as key contributors to the disease.
Background and Objective
- Equine Degenerative Myeloencephalopathy is a commonly occurring neurological condition in young horses, which progressively results in the weakening of their muscular and nervous systems. The key motive of this article is to delve deeper into the causes and manifestations of EDM, as well as treatment methodologies that can be employed.
Symptoms and Diagnosis of EDM
- The primary symptoms of EDM are characterized by an insidious development of symmetric ataxia, an inability to coordinate muscle movements. Losing the cutaneous trunci reflex, a kind of skin reflex, or having decreased responses to the slap test, also raise the suspicion of the presence of this disease.
- Additional supporting factors that could strengthen the diagnosis include a family history of the disorder, inadequate exposure to green pastures, and possible contact with wood preservatives or insecticides.
Pathogensis and Predisposition
- The article identifies dietary Vitamin E deficiency and hereditary factors as crucial elements contributing to the development of the disease.
- The histological examination reveals specific changes: prominent axonal and dendritic swelling, mild glial proliferation, and neuronal depletion and atrophy with lipofuscin-like pigment accumulation. These changes are characteristic of neuraxonal dystrophy, a nerv cell degeneration condition, suggesting the grave nature of the disease.
Treatment and Prognosis
- Horses that are diagnosed with or predisposed to EDM should receive supplementation with alpha-tocopherol acetate, a form of Vitamin E. However, restoration of normal muscular and nervous functions generally comes with long-term treatment.
- Regardless, the prognosis for complete recovery from EDM is generally not favorable, signifying the severity and stubbornness of the disease.
Cite This Article
APA
Beech J.
(1987).
Equine degenerative myeloencephalopathy.
Vet Clin North Am Equine Pract, 3(2), 379-383.
https://doi.org/10.1016/s0749-0739(17)30680-6 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Central Nervous System Diseases / etiology
- Central Nervous System Diseases / pathology
- Central Nervous System Diseases / veterinary
- Horse Diseases / etiology
- Horse Diseases / pathology
- Horses
- Nerve Degeneration
References
This article includes 18 references
Citations
This article has been cited 3 times.- Finno CJ, Famula T, Aleman M, Higgins RJ, Madigan JE, Bannasch DL. Pedigree analysis and exclusion of alpha-tocopherol transfer protein (TTPA) as a candidate gene for neuroaxonal dystrophy in the American Quarter Horse. J Vet Intern Med 2013 Jan-Feb;27(1):177-85.
- Adams AP, Collatos C, Fuentealba C, Illanes O, Blanchard R. Neuroaxonal dystrophy in a two-year-old quarter horse filly. Can Vet J 1996 Jan;37(1):43-4.
- Cummings JF, de Lahunta A, Mohammed HO, Divers TJ, Summers BA, Valentine BA, Jackson CA. Endothelial lipopigment as an indicator of alpha-tocopherol deficiency in two equine neurodegenerative diseases. Acta Neuropathol 1995;90(3):266-72.
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