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- Neuronal Ceroid Lipofuscinosis 1, NCL 1
Neuronal Ceroid Lipofuscinosis 1, NCL 1
PPT1 Exon 8, Dachshund Variant 1
- Multisystem
This condition affects how cells recycle waste. When waste accumulates, nerve cells are damaged, resulting in neurological signs that typically begin in younger dogs and worsen over time.
Dachshunds with this mutation are reported to show symptoms around nine months of age.
Talk to your vet about your dog’s NCL result so you can work together to plan ongoing care and monitoring. Note any changes in their coordination, mobility, or behavior.
Keep your dog’s environment calm and consistent. Use slings, harnesses, or supportive devices as needed to help with mobility, and place rugs or mats on slippery floors to prevent falls.
Encourage gentle, food-based activities such as treat searches or puzzle toys to help your dog stay mentally engaged without overexertion.
Help your dog feel secure by keeping furniture in familiar places, using non-slip mats, and maintaining predictable daily routines.
A mutation in the PPT1 gene was first identified in Dachshunds with an early onset form of NCL. PPT1 codes for the enzyme palmitoyl protein thioesterase, which plays a role in lysosomal protein degradation; this mutation leads to a nonfunctional enzyme, leading to neurologic signs.
Penetrance: This disease is inherited in an autosomal recessive manner, meaning that affected dogs must have two copies of the mutation to show clinical signs.
- Gene
- PPT1 (Exon 8)
- Inheritance type
- recessive
- Clinical category
- Multisystem
Citations
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