VNDL
  • Home
  • Search
  • Contact
  • More
    • Methodology
    • Video Library
    • External Resources
    • FAQ
<Return to Disease List
Neuronal Ceroid Lipofuscinosis​
  • Description
  • Signalment
  • Clinical Features
  • Neurolocalization
  • Genetics
<
>
Neuronal ceroid lipofuscinosis are a group of lysosomal storage disorders characterized by intracellular accumulations resulting in progressive neuronal degeneration.
Age of Onset: 1-9 years (most are less than 2 years of age)
Sex Predisposition: Any sex of dog can be affected
Clinical Course:
​Clinical signs slowly progress over time. After years of progression the dog may be unable to stand or walk.

Clinical Signs:
Behavioral/Mental Awareness
Seizures
Personality change
Aggression
Hyperactivity
Loss of learned behavior
Self-mutilation

Movement
Ataxia
Head tremors
Tetraparesis

Proprioception
Proprioceptive deficits

Cranial Nerves
Visual impairment (central blindness)
​Absent menace response
Absent dazzle response
Bilateral ventral strabismus
Intracranial - diffuse
Autosomal recessive; deletion of the CLN8 gene

For breed specific genetic testing follow the links below:
https://www.animalabs.com/shop/dog/neuronal-ceroid-lipofuscinosis-type-8-ncl8--alpine-dachsbracke/
​​https://www.genomia.cz/en/test/ncl8-dachsbracke/
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