PRA-RCD4 – Progressive Retinal Atrophy

43.90 € inc. Vat

Acronyms: PRA-RCD4
Gene: C2orf71
Mutation: Insertion
Mode of inheritance: Autosomal recessive
Breeds: Gordon Setter, Irish Setter, English Setter, Tibetan Terrier, Standard Poodle, Australian Cattle Dog, Polish Lowland Sheepdog, Small Munsterlander

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Product Description

PRA-RCD4 – Progressive retinal atrophy

PRA-RCD4 is an eye disorder, which belongs in progressive retinal atrophy group of disorders. Progressive retinal atrophy (PRA) comprises autosomal recessively inherited diseases that lead to degeneration of retinal photoreceptor cells in dogs and other pets. In general, these diseases are characterized by disturbance of dark vision, visual field defects, and abnormalities in the electroretinogram, which can progress to blindness. It appears in both eyes simultaneously. The age of onset and rate of retinal degeneration varies between the different forms of the conditions. Some forms of PRA are common to multiple dog breeds, while others are recognized in just a single breed. PRA appears in most dog breeds, but also in mixed breed dogs. Almost all PRA disorders are recessively inherited, with exceptions of dominant and X-linked PRA inheritance in few breeds, such as Old English Mastiffs, Bullmastiffs, Siberian Husky and Samoyed.

Rods are important for vision in dim light, or also night vision. Because of that, PRA with its rode degeneration leads to night blindness. In the researches, it is estimated that PRA causes death of around 95% of the dog’s photoreceptors. For dog owners or breeders, PRA is recognized by ”glow” or ”increased shine” in the eyes. The disease can progress, from initial stage of night blindness to advanced stage of PRA which causes full blindness in the dog. The advanced stage of PRA usually occurs within one year, since the appearance of the first symptoms.

After the death of rods, oxygen is still being delivered to the dead roads, which they cannot use. This excessive oxygen is toxic and it causes oxidative damage and consequently, cone death. The death of retinal tissue causes release of toxic products of cells. They are being absorbed by the lens, which causes lens damage and also cataract development.

In 2011. a specific form of PRA has been identified in the Gordon Setter. It is referred to as PRA-RCD4, in order to distinguish it from other forms of PRA, which are caused by different mutations. The mutation in this form of PRA is located in the rcd4 gene. PRA-RCD4 is also known as Late Onset PRA (LOPRA). In average, the symptoms occur and this form of PRA is diagnosed in affected dogs at 10 years of age, although it can vary between different breeds.


PRA-RCD4 is inherited in an autosomal recessive pattern. It is caused by a mutation in the C2orf71 gene. In case of showing the signs of PRA-RCD4, the healthy parents of an affected dog are obligate heterozygotes, and therefore carry one mutant allele. Heterozygotes have no symptoms. At conception, each cub has a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier.

There is no cure for PRA, and only way to prevent it, is to breed dogs which are not carriers of the mutation. Defected genes for autosomal recessive disease can be passed for many generations without affected individuals occurring until two carriers are bred to one another. The only way to find out if there is a chance of getting an affected puppy is to do PRA-RCD4 genetic testing.


Downs, LM, (2013.): Late-onset progressive retinal atrophy in the Gordon and Irish Setter breeds is associated with a frameshift mutation in C2orf71. Anim Genet. 44(2):169-77.