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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
Ataxia
Tetraplegia
​
Muscle spasms
“Swimming” motion of the limbs
Tremor

Cranial Nerves
Nystagmus
​Amblyopia (lazy eye)

Intracranial
Autosomal recessive inheritance
To read more about this disease click below:
References
Picture
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