• Medientyp: E-Artikel
  • Titel: Polyneuropathy in Young Siberian Huskies Caused by Degenerative and Inflammatory Diseases
  • Beteiligte: Jahns, Hanne; Vernau, Karen M.; Nolan, Catherine M.; O’Neill, Emma J.; Shiel, Robert E.; Shelton, G. Diane
  • Erschienen: SAGE Publications, 2020
  • Erschienen in: Veterinary Pathology
  • Sprache: Englisch
  • DOI: 10.1177/0300985820934112
  • ISSN: 0300-9858; 1544-2217
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:p> Polyneuropathy is defined as the simultaneous dysfunction of several peripheral nerves. In dogs, a number of breeds are predisposed to a variety of immune-mediated and/or degenerative inherited forms of polyneuropathy, with laryngeal paralysis and/or megaesophagus as important clinical features of many of these conditions. This case series describes degenerative and inflammatory polyneuropathies in 7 young Siberian huskies that were categorized based on clinicopathological characteristics as follows: (1) slowly progressive laryngeal paralysis and megaesophagus caused by primary axonal degeneration with large fiber loss (n = 2); (2) slowly progressive polyneuropathy without megaesophagus or laryngeal paralysis caused by primary axonal degeneration with large fiber loss (n = 2); (3) acute inflammatory demyelinating neuropathy causing sensory, motor and autonomic nerve deficits (n = 2); and (4) ganglioradiculitis (sensory neuronopathy; n = 1). Based on the predominantly young age at onset, slow progression, relatedness of affected dogs, and clinical and pathological similarities with inherited neuropathies reported in other dog breeds, a hereditary basis for the degenerative polyneuropathies in Siberian huskies is suspected. However, 5 different mutations in 3 genes known to cause polyneuropathy in other dog breeds ( NDRG1, ARHGEF10, or RAB3GAP1) were not detected in the affected Siberian huskies suggesting that more genetic variants remain to be identified. This study highlights the varied underlying lesions of polyneuropathies in young Siberian huskies. </jats:p>
  • Zugangsstatus: Freier Zugang