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Equine Neuroaxonal Dystrophy and Degenerative Myeloencephalopathy
Carrie J Finno1, Amy L Johnson2
1Department of Veterinary Population Health and Reproduction, School of Veterinary Medicine, University of California Davis, Room 4206 Vet Med 3A One Shields Avenue, Davis, CA 95616, USA.
The Veterinary Clinics of North America. Equine Practice
|July 10, 2022
Summary
Equine neuroaxonal dystrophy (eNAD) and equine degenerative myeloencephalopathy (EDM) are inherited neurological diseases in horses. Vitamin E may influence the severity of these conditions, impacting clinical signs like ataxia.
Area of Science:
- Veterinary Neurology
- Equine Genetics
- Animal Pathology
Background:
- Equine neuroaxonal dystrophy (eNAD) and equine degenerative myeloencephalopathy (EDM) are distinct pathological classifications of a similar neurodegenerative condition in horses.
- Both conditions manifest clinically with ataxia, often with an insidious onset during early development, but can also present later with behavioral changes.
Purpose of the Study:
- To summarize the current understanding of equine neuroaxonal dystrophy (eNAD) and equine degenerative myeloencephalopathy (EDM).
- To highlight the diagnostic criteria and potential genetic and environmental factors influencing these equine neurological disorders.
Main Methods:
- Histologic evaluation of the caudal medulla and cervicothoracic spinal cord is required for definitive diagnosis of eNAD/EDM.
- Review of existing evidence regarding the inheritance patterns and potential environmental modifiers of eNAD/EDM.
Main Results:
- eNAD and EDM are characterized by neuroaxonal degeneration in specific regions of the horse's central nervous system.
- Clinical presentation commonly includes ataxia, with variations in onset and additional signs like behavioral changes.
- Histopathology remains the gold standard for diagnosis.
Conclusions:
- eNAD/EDM are likely inherited equine neurological diseases.
- Vitamin E is implicated as an environmental factor that may modify the severity of the disease phenotype.
- Further research into genetic and nutritional factors is warranted for improved management and potential prevention strategies.
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