Awaiting product image

€57,48 €47,50 excl. VAT

H306

Canine Multifocal Retinopathy (CMR) is an eye disorder characterised by multiple areas of retinal degenerationm, potentially causing a loss of central vision.

10 working days

Specifications

Breeds

Gene

Organ

specimen

Swab, Blood EDTA, Blood Heparin, Semen, Tissue
Mode of Inheritance

Chromosome

Also known as

General information

Canine Multifocal Retinopathy (CMR) is an eye disorder characterised by multiple areas of retinal degenerationm, potentially causing a loss of central vision. This variant of the disorder, CMR3, occurs specifically in the Lapponian Herder, and is caused by a recessive mutation to the gene BEST1.

Clinical features

On veterinary examination, clinical signs of CMR include multiple tan-pink subretinal patches ("blisters") in both the tapetal and the non-tapetal fundus along with focal areas of tapetal hyper-reflectivity. The disorder does not typically lead to blindness.

Additional information

References

Pubmed ID:

Omia ID: 1554

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.

Related products