VNDD
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Hereditary Quadriplegia and Amblyopia
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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This disease is caused by an autosomal recessive mutation leading to cerebellar degeneration causing associated clinical signs.
Age of Onset: Greater than 10 days of age
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs may progress with age
Clinical Signs:
Behavioral/Mental Awareness
Seizures

Movement
Astasia
Ataxia
Tetraplegia (“Quadriplegia”
Spams (Muscle)
“Swimming” motion of all limbs
Tremor

Cranial Nerves
Rotary nystagmus
Amblyopia
Intracranial
Autosomal recessive inheritance
To read more about this disease click below:
References
Picture
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