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Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats
BACKGROUND: Reports of motor polyneuropathies in young cats are scarce. Further, in‐depth electrophysiologic evaluation to confirm a motor polyneuropathy in young cats of various breeds other than 2 Bengal cats is lacking. HYPOTHESIS/OBJECTIVES: To confirm a motor polyneuropathy in young cats of var...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895637/ https://www.ncbi.nlm.nih.gov/pubmed/25231268 http://dx.doi.org/10.1111/jvim.12439 |
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author | Aleman, M. Dickinson, P.J. Williams, D.C. Sturges, B.K. LeCouteur, R.A. Vernau, K.M. Shelton, G.D. |
author_facet | Aleman, M. Dickinson, P.J. Williams, D.C. Sturges, B.K. LeCouteur, R.A. Vernau, K.M. Shelton, G.D. |
author_sort | Aleman, M. |
collection | PubMed |
description | BACKGROUND: Reports of motor polyneuropathies in young cats are scarce. Further, in‐depth electrophysiologic evaluation to confirm a motor polyneuropathy in young cats of various breeds other than 2 Bengal cats is lacking. HYPOTHESIS/OBJECTIVES: To confirm a motor polyneuropathy in young cats of various breeds. ANIMALS: Five young cats with heterogenous chronic or relapsing episodes of weakness. METHODS: Retrospective case series. Cats were presented for evaluation of generalized neuromuscular disease and underwent electrophysiologic examination including electromyography, nerve conduction, and repetitive nerve stimulation. Minimum database and muscle and nerve biopsy analyses were carried out. Descriptive statistics were performed. RESULTS: Disease onset was at 3 months to 1 year of age and in 5 breeds. The most common clinical sign (5 of 5 cats) was weakness. Additional neurologic deficits consisted of palmigrade and plantigrade posture (4/4), low carriage of the head and tail (4/4), and variable segmental reflex deficits (5/5). Motor nerve conduction studies were abnormal for the ulnar (4/4), peroneal (5/5), and tibial (2/2) nerves (increased latencies, reduced amplitudes, slow velocities). A marked decrement was observed on repetitive nerve stimulation of the peroneal nerve in 3 cats for which autoimmune myasthenia gravis was ruled out. All sensory nerve conduction studies were normal. Histologic evaluation of muscle and nerve biopsies supported heterogenous alterations consistent with motor polyneuropathy with distal nerve fiber loss. CONCLUSIONS AND CLINICAL IMPORTANCE: Heterogenous motor polyneuropathies should be considered in young cats of any breed and sex that are presented with relapsing or progressive generalized neuromuscular disease. |
format | Online Article Text |
id | pubmed-4895637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-48956372016-06-22 Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats Aleman, M. Dickinson, P.J. Williams, D.C. Sturges, B.K. LeCouteur, R.A. Vernau, K.M. Shelton, G.D. J Vet Intern Med Standard Articles BACKGROUND: Reports of motor polyneuropathies in young cats are scarce. Further, in‐depth electrophysiologic evaluation to confirm a motor polyneuropathy in young cats of various breeds other than 2 Bengal cats is lacking. HYPOTHESIS/OBJECTIVES: To confirm a motor polyneuropathy in young cats of various breeds. ANIMALS: Five young cats with heterogenous chronic or relapsing episodes of weakness. METHODS: Retrospective case series. Cats were presented for evaluation of generalized neuromuscular disease and underwent electrophysiologic examination including electromyography, nerve conduction, and repetitive nerve stimulation. Minimum database and muscle and nerve biopsy analyses were carried out. Descriptive statistics were performed. RESULTS: Disease onset was at 3 months to 1 year of age and in 5 breeds. The most common clinical sign (5 of 5 cats) was weakness. Additional neurologic deficits consisted of palmigrade and plantigrade posture (4/4), low carriage of the head and tail (4/4), and variable segmental reflex deficits (5/5). Motor nerve conduction studies were abnormal for the ulnar (4/4), peroneal (5/5), and tibial (2/2) nerves (increased latencies, reduced amplitudes, slow velocities). A marked decrement was observed on repetitive nerve stimulation of the peroneal nerve in 3 cats for which autoimmune myasthenia gravis was ruled out. All sensory nerve conduction studies were normal. Histologic evaluation of muscle and nerve biopsies supported heterogenous alterations consistent with motor polyneuropathy with distal nerve fiber loss. CONCLUSIONS AND CLINICAL IMPORTANCE: Heterogenous motor polyneuropathies should be considered in young cats of any breed and sex that are presented with relapsing or progressive generalized neuromuscular disease. John Wiley and Sons Inc. 2014-09-17 2014 /pmc/articles/PMC4895637/ /pubmed/25231268 http://dx.doi.org/10.1111/jvim.12439 Text en Copyright © 2014 by the American College of Veterinary Internal Medicine |
spellingShingle | Standard Articles Aleman, M. Dickinson, P.J. Williams, D.C. Sturges, B.K. LeCouteur, R.A. Vernau, K.M. Shelton, G.D. Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats |
title | Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats |
title_full | Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats |
title_fullStr | Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats |
title_full_unstemmed | Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats |
title_short | Electrophysiologic Confirmation of Heterogenous Motor Polyneuropathy in Young Cats |
title_sort | electrophysiologic confirmation of heterogenous motor polyneuropathy in young cats |
topic | Standard Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895637/ https://www.ncbi.nlm.nih.gov/pubmed/25231268 http://dx.doi.org/10.1111/jvim.12439 |
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