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#lapponianherderdog

Canine Multifocal Retinopathy Lapponian Herders (CMR3)

Micah Halpern · September 27, 2022 ·

GenSol Diagnostics is now offering Canine Multifocal Retinopathy testing specifically for Lapponian Herder Dogs.

The canine multifocal retinopathy mutation causes raised lesions to form on the retina which alters the appearance of the eye but usually does not affect sight. The lesions may disappear, or may result in minor retinal folding. Symptoms of the mutation usually appear when a puppy is only a few months old, and generally do not worsen over time. The genetic test for CMR is valuable for identifying the cause of a retinal deformation. Given the exact genetic diagnosis, the owner can be reassured that there probably will be little or no vision loss due to this condition. While the CMR1, CMR2 and CMR3
mutations are in the same gene, they are breed specific and testing for only one is required.

Breed Specific Canine Multifocal Retinopathy

  • The CMR3 mutations is specific for the Lapponian Herder breed.
  • The CMR2 mutation is specific for the Coton de Tulear breed.
  • All other breeds should test for the CMR1 mutation.

Additional GenSol Tests for Lapponian Herder Dogs

  • DEGENERATIVE MYELOPATHY (DM)
  • PROGRESSIVE ROD-CONE DEGENERATION (PRA-PRCD)
  • PROGRESSIVE RETINAL ATROPHY (PRA-LH)

Visit our Lapponian Herder Dog Disease page for easy access to ordering.

Other Helpful Information on Lapponian Herder Dogs

  • American Kennel Club – Lapponian Herder Dog
  • PetKeen – Lapponian Herder Dog
  • Wikipedia – Lapponian Herder Dog

Article List, Canine Genetics, Dog Breeding, Pet Health, The Doggie Bag, Uncategorized #lapponianherder, #lapponianherderdog, #Veterinary Medicine, #vettechlife, Affordable Canine Genetic Testing, Canine Genetics, Canine Multifocal Retinopathy, Dog Breeders, Dog Health, Gensol Diagnostics

Progressive Retinal Atrophy for Lapponian Herders (PRA-LH)

Micah Halpern · May 18, 2022 ·

Progressive Retinal Atrophy (PRA) is a category of disorders where the retinal cells in a dog’s eye degenerate and die eventually leading to complete blindness. A type of PRA specific to Lapponian Herders is due to a mutation in the IFT122 gene that leads to adult-onset eye disease. Symptoms will typically appear on average at 5 years old and is usually diagnosed anywhere from 5 to 12 years of age. Initial symptoms include vision difficulties in dim light often referred to as night blindness. As the disease progresses, the affected dog will continue to suffer loss of night vision which then progresses to visual deficits in brighter light and can eventually lead to total blindness. It is important to note that not all cases of PRA in Lapponian Herders are caused by this particular mutation.

Additional GenSol Tests for Lapponian Herder Dogs

  • DEGENERATIVE MYELOPATHY (DM)
  • PROGRESSIVE ROD-CONE DEGENERATION (PRA-PRCD)

Visit our Lapponian Herder Dog Disease page for easy access to ordering.

Other Helpful Information on Lapponian Herder Dogs

  • American Kennel Club – Lapponian Herder Dog
  • PetKeen – Lapponian Herder Dog
  • Wikipedia – Lapponian Herder Dog

Article List, Canine Genetics, Dog Breeding, Pet Health, The Doggie Bag, Uncategorized #lapponianherderdog, #Veterinary Medicine, #vettechlife, Affordable Canine Genetic Testing, Canine Genetics, Dog Breeders, Dog Health, Gensol Diagnostics

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