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Multifokale Retinopathie 3 (CMR3) option-set-443684-checkbox-1 balance loss and seizures

SKU: 47342004295
4.2

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Description

balance loss and seizures

Mutation: KCNJ10 gene

The clinical signs appear around 3–12 months of age in most dogs and progresses before the age of two years

Mutation: PLG gene

The clinical improvement of affected pups can shortly be achieved with albuterol

Multifokale Retinopathie 3 (CMR3) option-set-443684-checkbox-1 balance loss and seizuresCanine multifocal retinopathies (CMR) are a group of inherited eye diseases. The diseases were reported in mastiff related breeds (CMR1), Coton de Tulear (CMR2) and in Lapponian herder (CMR3). CMR1 is found in different dog breeds, whereas CMR2 and CMR3 are so far exclusive to a single dog breed each. While exhibiting similar clinical symptoms comparable to CMR1 and CMR2, CMR3 is predicted to be based on a distinctly different molecular mechanism.

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