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Dog DNA testing illustration

Degenerative Myelopathy Exon 2 (DM Exon 2)

Kodas: H673

74,72 €

Mėginio duomenys

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Short description

Canine Degenerative Myelopathy (DM) is an incurable progressive neurodegenerative disease of the spinal cord.

General information

Canine Degenerative Myelopathy (DM) is an incurable progressive neurodegenerative disease of the spinal cord. Neurodegenerative diseases are characterised by progressive loss of neurons in the central nervous system (CNS) which leads to deficiencies in function. In the case of DM, the affected region is the spinal cord, which results in ataxia (a loss of coordination). DM is similar in many ways to Amyotrophic Lateral Sclerosis (ALS) in humans.

This variant of the disease, sometimes designated as SOD1A or as Degenerative Myelopathy Exon 2, occurs in many different breeds. It is caused by an autosomal recessive with incomplete penetrance mutation to the gene SOD1. Although the mutation is found in many breeds, the disease is rarely diagnosed in breeds or in mixed-breed dogs other than those mentioned for this test. A related variant specific to the Bernese Mountain Dog has also been observed. When testing a Bernese Mountain Dog for DM, it is important to test for both of these variants, as opposed to only one.

For DM in Pembroke Welsh Corgis there are also multiple Degenerative Myelopathy Risk Modifiers (DMRM) descibed in literature. These SP110 mutations are available for testing in a different package.

Specifications

Breeds

American Water Spaniel, Borzoi, Canaan Dog, Czechoslovakian Vlcak, Glen of Imaal Terrier, Huntaway, New Zealand Heading Dog, Poodle (Standard), Romanian Mioritic Shepherd Dog, Schnauzer (Giant), Schnauzer (Miniature), Smooth Collie, Tamaskan, Wire Fox Terrier, Airedale Terrier, Komondor, American Eskimo dog, American Pit Bull Terrier, Australian Shepherd, Bernedoodle, Bernese Mountain dog, Bloodhound, Border Collie, Boston Terrier, Boxer, Boykin Spaniel, Cardigan Welsh Corgi, Cavalier King Charles Spaniel, Chesapeake Bay Retriever, English Springer Spaniel, French Bulldog, German Shepherd, Golden Retriever, Great Pyrenees, Hovawart, Irish Setter, Jack Russell Terrier, Kerry Blue Terrier, Kuvasz, Labrador Retriever, Nova Scotia Duck Tolling Retriever, Pembroke Welsh Corgi, Pug, Rhodesian Ridgeback, Rottweiler, Rough Collie, Saint Bernard, Scottish Deerhound, Shetland Sheepdog, Siberian Husky, Soft Coated Wheaten Terrier, Tibetan Terrier, White Swiss shepherd

Gene

SOD1

Chromosome

31

Mutation

c.118G>A

Organ

Nervous System

Specimen

Swab, Blood EDTA, Blood Heparin, Semen, Tissue

Mode of Inheritance

Autosomal Recessive with Incomplete Penetrance

Also known as

DM

Clinical features

Most dogs are at least 8 years of age at the onset of the first clinical signs, which include hyporeflexia and ataxia of the pelvic with progression over time to complete paralysis and incontinence.

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: 19188595

Year published: 2009

Omia ID: 263

Omia variant ID:

Turnaround information

  • 15 working days
  • This test is performed by an external laboratory.
  • CombiBreed takes care of the mediation between you as a customer and the external laboratory.