VNDL
  • Home
  • Search
  • Contact
  • More
    • Methodology
    • Video Library
    • External Resources
    • FAQ
<Return to Disease List
Hereditary Polyneuropathy/Neuropathy​
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
<
>
Hereditary polyneuropathy is an idiopathic degeneration of nerves often characterized by axonal degeneration and hypomyelination.
Age of Onset: 7-18 months of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
Clinical signs worsen over time
Clinical Signs:
Movement
Collapse
Progressive paraparesis to tetraparesis
Bunny-hopping gait
Inability to walk up stairs or jump
Difficulty standing


Proprioception
Proprioceptive deficits 

Spinal Reflexes
Decreased spinal reflexes
Reduced appendicular muscle tone

Special Functions (e.g. respiration; urination)
Exercise intolerance
Inspiratory stridor
Megaesophagus

Muscle Atrophy
General muscle atrophy (greater in the distal appendicular muscles)
Atrophy of muscles of mastication (CN V) and glossal muscles (CN XII)

Other
Abnormal vocalization
Paraspinal hyperesthesia
Peripheral nerve/neuromuscular
Autosomal recessive mutation in NDRG1 gene

For breed specific genetic tests, follow the links below:

https://canine-genetics.umn.edu/canine-genetic-testing/alaskan-malamute-polyneuropathy
https://vgl.ucdavis.edu/test/alaskan-malamute-polyneuropathy
To read more about this disease click below:
References
Picture
Contact us:
[email protected]

Privacy Policy
Terms and Conditions​
Disclaimer
  • Home
  • Search
  • Contact
  • More
    • Methodology
    • Video Library
    • External Resources
    • FAQ