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Progressive Retinal Atrophy (PRA-prcd)
PRA-prcd is progressive, and late-onset, where retina cells are lost slowly. This initially causes problems seeing in dim light, usually around ages 3-5, though diagnosis by an ophthalmologist can be earlier, around 1-2 years. It can progress to complete blindness is some dogs, but not all cases. This disease is seen in many breeds and crosses.
  Discussion

Key Comment: Multiple research sources indicate that this form of PRA-prcd could be present in many breeds, and testing could be relevant widely across a large number of different breeds of dog, many of which are terriers or breeds with terrier co-ancestry, but some of which have more diverse origins. Research indicates that the mutation is present at varying breed-specific frequency, but that testing and applying the test results can lead to signifigant reduction in the disease.

PRA-prcd is progressive, and late-onset, where retina cells are lost slowly. This initially causes problems seeing in dim light, usually around ages 3-5, though diagnosis by an ophthalmologist can be earlier, around 1-2 years. It can progress to complete blindness is some dogs, but not all cases. This disease is seen in many breeds and crosses.

Canine progressive rod-cone degeneration (prcd) is a retinal disease previously mapped to a broad, gene-rich centromeric region of canine chromosome 9. An allelic disorders present in multiple breeds, and crosses of those breeds. Research strongly suggests that a common ancestor transmitted the prcd disease allele to many of the modern dog breeds. Diagnosis of prcd is based on a combination of clinical examination, including indirect ophthalmoscopy and electroretinography, and retinal morphology. Retinal photoreceptor abnormalities are visible in animals 14 weeks of age and older using high-resolution optical microscopy.

  Genetics
Inheritance
AR
OMIA
001298
OMIA Variant
000076
OMIA URL
https://omia.org/OMIA001298/9615/
OMIN
610599
Gene
PRCD
Variants
c.5G>A, G1298A, c.2685delA, c.2687_2688insTAGCTA
Variants Comments
Test has been reported as being offered as a linkage/marker test, from some GTPs
  Testing
Test Types
Genetic-Genomic
Opthal
Assessments
Eye / Ophthalmologist Exam
Specific Genetic Test
Assays
Linkage
Direct Mutation
Connections
  • Updated
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