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Congenital Myasthenic Syndrome (Discovered in the Devon Rex and Sphynx)

Congenital Myasthenic Syndrome (CMS) is a condition that causes muscle weakness and fatigue.

Found in

1 in 450 cats

in our testing

Key Signs

Muscular weakness, Fatigue, Megaesophagus, Difficulty swallowing

Age of Onset

0 to 2 yrs

Juvenile onset

Inheritance

Autosomal Recessive

For autosomal recessive disorders, cats with two copies of the variant are at risk of developing the condition. Cats with one copy of the variant are considered carriers and are usually not at risk of developing the disorder. However, carriers of some complex variants grouped in this category may be associated with a low risk of developing the disorder. Individuals with one or two copies may pass the disorder-associated variant to their kittens if bred.

Likelihood of the Condition

High likelihood

At risk cats are highly likely to show signs of this disease in their lifetime.

What to Do

Here’s how to care for a cat with CMS

Partner with your veterinarian to make a plan regarding your cat’s well-being, including any insights provided through genetic testing. If your pet is at risk or is showing signs of this disorder, then the first step is to speak with your veterinarian.

For Veterinarians

Here’s what a vet needs to know about CMS

Myasthenic syndromes are hereditary diseases caused by defective signal transmission in the neuromuscular junction. In the Sphynx and Devon Rex breeds, the disease is caused by the deficiency of alpha-dystroglycan expression in the neuromuscular synapses which results in reduced activity of acetylcholinesterase. Affected cats present with progressive muscular signs such as fatigue, reduced activity, generalized skeletal muscle weakness, and muscle tremors after exercise. Functional deficiency in the limb-girdle and axial musculature can lead to gait abnormalities, protrusion of the scapulae, and ventroflexion of the head and neck. Affected cats may also present with megaesophagus and can have difficulty swallowing which may lead to asphyxiation or aspiration pneumonia. Clinical signs are typically visible in kittens before five months of age and may be evident in some individuals as young as three weeks of age. Severity of clinical signs can vary and, while the disorder is slowly progressive, occasional cases do become static.

Upon initial observation of clinical signs, affected cats should be closely monitored to assess welfare and devise a supportive care treatment plan. Difficulty swallowing is a significant concern and elevation of food and water bowls may help to reduce the risk of asphyxiation or aspiration pneumonia. Affected cats experiencing progressive difficulties with swallowing are often euthanized for welfare reasons.

For Breeders

Planning to breed a cat with this genetic variant?

There are many responsibilities to consider when breeding cats. Regardless of test results it is important that your cat is in good general health and that you are in a position to care for the kittens if new responsible owners are not found. For first time or novice breeders, advice can be found at most cat registry websites.

This disease is autosomal recessive meaning that two copies of the mutation are needed for disease signs to be shown. A carrier cat with one copy of the CMS mutation can be safely bred with a clear cat with no copies of the CMS mutation. About half of the kittens will have one copy (carriers) and half will have no copies of the CMS mutation. Kittens in a litter which is expected to contain carriers should be tested prior to breeding. Carrier to carrier matings are not advised as the resulting litter may contain affected kittens. Please note: It is possible that disease signs similar to the ones caused by the CMS mutation could develop due to a different genetic or clinical cause.

Technical Details

Gene COLQ
Variant G>A
Chromosome C2
Coordinate 135,068,287

All coordinates reference FelCat9.0

References & Credit

Credit to our scientific colleagues:

Abitbol, M., Hitte, C., Bossé, P., Blanchard-Gutton, N., Thomas, A., Martignat, L., Blot, S., & Tiret, L. (2015). A COLQ missense mutation in Sphynx and Devon Rex cats with congenital myasthenic syndrome. PLoS ONE, 10(9). View the article