Common Symptoms
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type) is an inherited muscle disease in dogs. Affected dogs present around 3 to 4 months of age with deformed limbs and hyperflexion of the joints, most notably of the wrist (carpus) and the ankle (hock) giving the dog a flatfooted stance. Affected dogs may develop muscle Atrophy over time and have an abnormal gait. The disease is slowly progressive, and dogs can live many years before the disease becomes severe enough to warrant humane euthanasia.
Testing Tips
Genetic testing of the COL6A2 gene will reliably determine whether a dog is a genetic Carrier of Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type, Variant 2). This disease is inherited in an Autosomal Dominant manner meaning that dogs only need to inherit one copy of the mutated gene to develop the disease. Each pup that is born to a parent carrying one copy of the Mutation has a 50% chance of inheriting one copy of the COL6A3 gene mutation and being at-risk for the disease. Reliable genetic testing is important for determining breeding practices. In order to eliminate this mutation from breeding lines and to avoid the potential of producing affected pups, breeding of known carriers to each other is not recommended. Dogs that are not carriers of the mutation have no increased risk of having affected pups.
There may be other causes of this condition in dogs and a normal result does not exclude a different mutation in this gene or any other gene that may result in a similar genetic disease or trait.
References
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Bolduc V, Minor KM, Hu Y, Kaur R, Friedenberg SG, Van Buren S, Guo LT, Glennon JC, Marioni-Henry K, Mickelson JR, Bönnemann CG, Shelton GD. Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs. Neuromuscul Disord. 2020 May;30(5):360-367.
[PubMed: 32439203]
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Marioni-Henry K, Haworth P, Scott H, Witte P, Guo LT, Shelton GD. Sarcolemmal specific collagen VI deficient myopathy in a Labrador Retriever. J Vet Intern Med. 2014 Jan-Feb;28(1):243-9.
[PubMed: 24147807]