Progressive Retinal Atrophy Basenji Type (BAS-PRA)
Progressive retinal atrophy Basenji type (BAS-PRA) 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 (XLPRA) in few breeds, such as Old English Mastiffs, Bullmastiffs, Siberian Husky and Samoyed.
Characteristics and Symptoms
Rods are important for vision in dim light, or also night vision and 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 secondary cataracts or 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.
Progressive retinal atrophy Basenji type (BAS-PRA) is a late-onset form of PRA which has been identified in Basenji breeds. The first symptoms occur during dog’s 5 to 7 years of age. As other forms of PRA, the first symptoms of progressive retinal atrophy Basenji type are poor vision in dim light, which eventually progresses into complete blindness. By clinical signs and disease’s development, BAS-PRA resembles a lot to PRA-PRCD, but they differ in gene mutation which causes the disorder. PRA-PRCD mutation has not been found in BAS-PRA affected Basenji dogs.
The disorder is caused by a non-stop mutation in S-antigen gene (SAG). BAS-PRA is inherited as an autosomal recessive disorder. In case of showing the symptoms of BAS-PRA, 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 BAS-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 progressive retinal atrophy Basenji type genetic testing.