Progressive Retinal Atrophy, Early-Onset (Portuguese Water Dog Type)

Affected Genes: CCDC66
Inheritance: Autosomal Recessive
Mutation: chr20:33966929-33966930 (canFam4): -/T
Breed(s): Portuguese Water Dog

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Common Symptoms

Progressive retinal Atrophy, early‑onset (Portuguese Water Dog Type) is an early-onset eye disease affecting dogs. Affected dogs may present with vision problems between 2-3 years of age. Initial clinical signs of progressive retinal atrophy involve changes in reflectivity and appearance of a structure behind the Retina called the Tapetum that can be observed on a veterinary eye exam. Progression of the disease leads to thinning of the retinal blood vessels, signifying decreased blood flow to the retina. Affected dogs initially have vision loss in dim light (night blindness) and loss of peripheral vision, which may progress to complete blindness.


Testing Tips

Genetic testing of the CCDC66 gene in dogs will reliably determine whether a dog is a genetic Carrier of Progressive retinal Atrophy, early‑onset (Portuguese Water Dog Type). This disease is inherited in an Autosomal Recessive manner in dogs meaning that they must receive two copies of the mutated gene (one from each parent) to develop the disease. In general, carrier dogs do not have features of the disease but when bred with another carrier of the same Mutation, there is a risk of having affected pups. Each pup that is born to this pairing has a 25% chance of inheriting the disease and a 50% chance of being a carrier of the CCDC66 gene mutation. Reliable genetic testing is important for determining breeding practices. Because symptoms do not appear until adulthood, genetic testing should be performed before breeding. In order to eliminate this mutation from breeding lines and to avoid the potential of producing affected pups, breeding of known carriers to each other is not recommended. Portuguese Water Dogs that are not carriers of the mutation have no increased risk of having affected pups. However, because there are multiple types of PRA caused by mutations in other genes, a normal result in CCDC66 does not exclude PRA in a pedigree.


There may be other causes of this condition in dogs and a normal result does not exclude a different mutation in this gene or any other gene that may result in a similar genetic disease or trait.


References

  • Murgiano, L., Becker, D., Spector, C. et al. CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs. Sci Rep 10, 21162 (2020). [PubMed: 33273526]