139,15 115,- excl. VAT

H801

Progressive Retinal Atrophy (PRA) is a large group of genetic diseases in which the retina gradually degenerates over time, causing a progressive loss of vision.

25 working days

€5,95 shipping and administration per order (incl. VAT)

Specifications

General information

Progressive Retinal Atrophy (PRA) is a large group of genetic diseases in which the retina gradually degenerates over time, causing a progressive loss of vision. This specific variant of the disorder is known as Rod-Cone Dysplasia type 2 (rcd2, or rcd2-PRA). Rcd2 is an autosomal recessive disorder, caused by a splicing mutation in the RD3 gene, that occurs in collies.

Clinical features

Night blindness is the first clinical sign, which can already be detected in 6 weeks old collies. The retinal dysfunction can be detected in 16 days old dogs by electroretinography. By the age of 2-2,5 months underdeveloped segments are visible. Both rods and cones are not developed in the outer segments. Therefore, the outer segments disappear in the affected retina. The rods en cones will degenerate, cones slower than rods. By the age of 6 to 8 months the dogs become completely blind.

Additional information

This test is performed by an external laboratory. CombiBreed takes care of the mediation between you as a customer and the external laboratory. In this case, CombiBreed cannot be held liable for the behaviour of the client and/or contractor.

References

Pubmed ID: 19130129

Omia ID: 1260

How does it work?

1. Select your product(s)

Select your single test, a CombiBreed Package or create your own Bundle.

2. Collect DNA sample

Collect DNA material as indicated with our products and send it to our laboratory.

3. Results

We handle your DNA sample with care and provide you with the results.

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