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Equine Neuroaxonal Dystrophy and Degenerative Myeloencephalopathy.
Finno, Carrie J; Johnson, Amy L.
Afiliação
  • Finno CJ; Department 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. Electronic address: cjfinno@ucdavis.edu.
  • Johnson AL; Department of Clinical Studies, University of Pennsylvania School of Veterinary Medicine- New Bolton Center, 382 West Street Road, Kennett Square, PA 19348, USA.
Vet Clin North Am Equine Pract ; 38(2): 213-224, 2022 Aug.
Article em En | MEDLINE | ID: mdl-35811203
ABSTRACT
Neuroaxonal degenerative disease in the horse is termed equine neuroaxonal dystrophy (eNAD), when pathologic lesions are localized to the brainstem and equine degenerative myeloencephalopathy (EDM) and degenerative changes extend throughout the spinal cord. Both pathologic conditions result in identical clinical disease, most commonly characterized by the insidious onset of ataxia during early development. However, later onset of clinical signs and additional clinical features, such as behavior changes, is also observed. A definitive diagnosis of eNAD/EDM requires histologic evaluation of the caudal medulla and cervicothoracic spinal cord. Strong evidence has suggested that eNAD/EDM is an inherited disorder and there seems to be a role for vitamin E acting as an environmental modifier to determine the overall severity of the phenotype of horses affected with eNAD/EDM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofias Neuroaxonais / Doenças dos Cavalos Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: Vet Clin North Am Equine Pract Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofias Neuroaxonais / Doenças dos Cavalos Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: Vet Clin North Am Equine Pract Ano de publicação: 2022 Tipo de documento: Article