Hereditary canine spinal muscular atrophy: canine motor neuron disease.

L. C. Cork, D. L. Price, J. W. Griffin, George Henry Sack

Research output: Contribution to journalArticle

Abstract

Motor neuron diseases, manifest as weakness and atrophy of skeletal muscles, occur in infancy, childhood, and adult life. Some forms of this disease are inherited. Motor neurons are selectively affected and exhibit cytoskeletal pathology, primarily enlargements of proximal axons by accumulations of transported neurofilaments. A motor neuron disease, hereditary canine spinal muscular atrophy, has been discovered in Brittany spaniels. The disease is inherited as an autosomal dominant characteristic and shows striking clinical and pathological features in common with human motor neuron disease. The availability of this excellent animal model of the human condition has allowed neurobiological investigations of the dynamics of structural and chemical pathologies of vulnerable neurons.

Original languageEnglish (US)
Pages (from-to)77-82
Number of pages6
JournalCanadian journal of veterinary research = Revue canadienne de recherche veterinaire
Volume54
Issue number1
StatePublished - Jan 1990

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Spinal Muscular Atrophy
Motor Neuron Disease
muscular atrophy
motor neurons
Canidae
dogs
Pathology
Intermediate Filaments
Motor Neurons
Atrophy
Axons
Skeletal Muscle
genetic disorders
infancy
Animal Models
atrophy
childhood
axons
skeletal muscle
Neurons

ASJC Scopus subject areas

  • veterinary(all)

Cite this

Hereditary canine spinal muscular atrophy : canine motor neuron disease. / Cork, L. C.; Price, D. L.; Griffin, J. W.; Sack, George Henry.

In: Canadian journal of veterinary research = Revue canadienne de recherche veterinaire, Vol. 54, No. 1, 01.1990, p. 77-82.

Research output: Contribution to journalArticle

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