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(Cerebellar) Neuroaxonal Dystrophy
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Neuroaxonal dystrophy is a progressive disorder characterized by accumulation of swollen axons distributed throughout the central nervous system.
Age of Onset: 1-2 years of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs worsen over 2-4 years
Clinical Signs:
Movement
Ataxia
Hypermetria
Head (Intention) tremor
Circling


Proprioception
General proprioception remains intact

Cranial Nerves
Menace deficit
Nystagmus (resting and/or positional)
Intracranial - Cerebellum and associated pathways
Unknown
To read more about this disease click below:
References
Picture
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