Intestinal Cobalamin Malabsorption (Australian Shepherd Type)

Other Names: Amnionless Deficiency, Cobalamin Deficiency, Imerslund-Grasbeck Syndrome, Vitamin B12 Deficiency
Affected Genes: AMN
Inheritance: Autosomal Recessive
Mutation:

Add To Cart Search Tests

Common Symptoms

Intestinal cobalamin malabsorption (Australian shepherd type) is an inherited disease affecting dogs. Affected dogs are unable to make adequate amounts of a protein that plays a role in absorption of certain nutrients from the intestinal tract and kidneys, including the B vitamin, cobalamin. Affected dogs have increased levels of methylmalonic acid in their urine (a sign of cobalamin deficiency) after weaning, but symptoms of disease may not be recognized by owners for months or years. Symptoms of disease include anorexia, lethargy, poor weight gain, poor muscle mass, and in rare circumstances, a severe neurological dysfunction called hepatic encephalopathy that can lead to altered mental state, seizures, coma and death. Affected dogs have an increase in certain proteins in their urine, and have decreased synthesis of blood cells resulting in Anemia and decreased numbers of neutrophils. Affected dogs require cobalamin supplementation for life that results in disease remission for most animals within a few weeks. Though not associated with clinical disease, affected dogs will continue to pass increased amounts of certain proteins in the urine even with cobalamin supplementation.

Breed-Specific Information for the Toy Australian Shepherd

Toy Australian shepherd is included as a breed susceptible to intestinal cobalamin malabsorption (Australian shepherd type) because of its close relatedness to the Australian shepherd breed, which is known to develop this disease due to Mutation of the AMN gene. The frequency of the causal mutation in the general toy Australian shepherd population is unknown.

Testing Tips

Genetic testing of the AMN gene in toy Australian shepherds will reliably determine whether a dog is a genetic Carrier of intestinal cobalamin malabsorption (Australian shepherd type). Intestinal cobalamin malabsorption (Australian shepherd type) is inherited in an Autosomal Recessive manner in dogs meaning that they must receive two copies of the mutated gene (one from each parent) to develop the disease. In general, carrier dogs do not have features of the disease but when bred with another carrier of the same Mutation, there is a risk of having affected pups. Each pup that is born to this pairing has a 25% chance of inheriting the disease and a 50% chance of inheriting one copy and being a carrier of the AMN gene mutation. 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. Toy Australian shepherds 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

  • Gold AJ, Scott MA, Fyfe JC. Failure to thrive and life-threatening complications due to inherited selective cobalamin malabsorption effectively managed in a juvenile Australian shepherd dog. Can Vet J. 2015 Oct;56(10):1029-34 [PubMed: 26483576]
  • He Q, Fyfe JC, Schaffer AA, Kilkenney A, Werner P, Kirkness EF, Henthorn PS. Canine Imerslund-Grasbeck syndrome maps to a region orthologous to HSA14q. Mamm Genome. 2003 Nov;14(11):758-64 [PubMed: 14722725]
  • He Q, Madsen M, Kilkenney A, Gregory B, Christensen EI, Vorum H, Hojrup P, Schaffer AA, Kirkness EF, Tanner SM, de la Chapelle A, Giger U, Moestrup SK, Fyfe JC. Amnionless function is required for cubilin brush-border expression and intrinsic factor-cobalamin (vitamin B12) absorption in vivo. Blood. 2005 Aug 15;106(4):1447-53 [PubMed: 15845892]