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Lysosomal Storage Disease (Galactosialidosis)
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
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Lysosomal storage disease is an idiopathic accumulation of metabolic byproducts within neuronal cells resulting in degeneration of neuronal tissue
Age of Onset: Adult onset (5+ years of age)
Sex Predisposition: Any sex of animal can be affected
Clinical Course:
​Clinical signs worsen over the course of several months
Clinical Signs:
Movement
Falling
Incoordination
Stumbling
Stiff hypermetric gait

Cranial Nerves
Positional vertical nystagmus

Spinal Reflexes
Exaggerated segmental reflexes​
Brain
Unknown
To read more about this disease click below:
References
Picture
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