This is a Multisystem condition.
Lagotto Storage Disease
What is Lagotto Storage Disease?
This form of lysosomal storage disease arises from a defect in the enzyme ATG4D, which plays a large role in the autophagy pathway. Autophagy describes the process by which the cell recycles damaged or malfunctioning parts of itself including old transport vesicles, organelles, and macromolecules. Loss of ATG4D stops the autophagy pathway in its tracks, causing cellular accumulation of old parts and eventual cellular malfunction and death.
What are the signs & symptoms that develop in affected dogs?
Ataxia, behavioral changes, and abnormal eye movements can be seen with this disorder.
When do signs and symptoms develop?
Signs can have a juvenile (4 months) to adult (4 years) onset.
How do vets diagnose this condition?
Genetic and laboratory testing used to diagnose this disease.
How is this condition treated?
There is no treatment except supportive care for the clinical signs the affected dog develops.
What actions should I take if my dog is affected?
- Focus on palliative therapies to increase your dog's comfort and quality of life.
