Progressive Retinal Atrophy (PRA) causes breakdown of the retina, which is a part of the eye essential for vision. This is a progressive, non-painful disease that affects both types of photoreceptors: rods and cones. Rods are essential for night vision and movement, while cones are used for day vision and color.
IMPG2
Autosomal recessive
PRA is a slowly progressive disease that causes vision loss in both eyes. This provides more opportunities for helping an affected dog adapt to its changing visual environment. Signs typically start with night blindness, which progresses to daytime vision loss.
Thorough examination of the eyes and clinical signs. A veterinary ophthalmologic exam can determine if there are changes in the eye that have or will lead to vision loss. Genetic testing is necessary to determine if there is an underlying genetic cause, which can assist veterinarians with diagnosis and help breeders identify affected and carrier dogs.
Lhaso Apso
Hitti-Malin RJ, Burmeister LM, Ricketts SL, Lewis TW, Pettitt L, Boursnell M, Schofield EC, Sargan D, Mellersh CS. A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs. BMC Genet. 2020 Sep 7;21(1):100. doi: 10.1186/s12863-020-00911-w. PMID: 32894063; PMCID: PMC7487703.
Disease diagnosis and treatment should always be performed by a veterinarian. The following information is for educational purposes only.
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