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Horse DNA testing illustration

Myosin Heavy Chain Myopathy (MYHM)

Code: P394

74,72 €

Sample details

One test – one sample. Animal and owner details are optional.

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Short description

Myosin-Heavy Chain Myopathy (MYHM) is a genetic muscle disease that can result in two distinct clinical disease presentations: Immune-Mediated Myositis (IMM) and Nonexertional Rhabdomyolysis.

General information

Myosin-Heavy Chain Myopathy (MYHM) is a genetic muscle disease that can result in two distinct clinical disease presentations: Immune-Mediated Myositis (IMM) and Nonexertional Rhabdomyolysis. They both involve muscle loss or damage and are linked to a mutation in the MYH1gene. This gene is involved in the normal functioning of the myosin protein in muscle cells. A horse with MYHM is prone to presenting with one or both MYHM diseases during their lifetime.
The IMM variant of MYHM is known to occur in the Quarter Horse, American Paint and Appaloosa and is a co-dominant mutation also known as dominant with variable penetrance, which means your horse only needs one copy to be affected, though some horses with the mutation may never experience symptoms. They must be exposed to a trigger to experience symptoms. Horses that are homozygous for the mutation are likely to experience more severe symptoms.

Specifications

Breeds

American Quarter Horse, American Paint Horse, Appaloosa

Gene

MYH1

Chromosome

11

Organ

Multiple systems

Specimen

Hair, Blood EDTA, Blood Heparin, Semen, Tissue

Mode of Inheritance

Autosomal Co-Dominant

Also known as

IMM

Clinical features

Immune-Mediated Myositis (IMM) is one form of clinical disease caused by MYHM, this results in infiltration of inflammatory cells, particularly lymphocytes, into muscle fibers and surrounding blood vessels. It is suspected to be the result of a response to a trigger. These triggers can include respiratory infections (especially Streptococcus), muscle damage, immune stimulants, vaccination against strangles, and muscle-damaging vaccinations. The immune system misinterprets the muscle cells as foreign and rapidly attacks them. Horses initially experience stiffness, weakness, and a decreased appetite followed by the rapid loss of 40% of muscle mass within 72 hours.

The second presentation of MYHM is Nonexertional Rhabdomyolysis and often presents as stiffness, like "tying up", and possible swelling of muscles along the back and haunches without exercise. Nonexertional rhabdomyolysis causes pain, muscle cramping, muscle damage and may or may not result in muscle loss.

Additional information

Horses with the mutation exposed to environmental triggers can develop symptoms of the disease. Not all environmental risk factors are currently known. Therefore, it is impossible to say if or how a horse with the MYHM mutation will be affected. Horses affected by IMM or Nonexertional Rhabdomyolysis can recover but may have more frequent episodes.

References

Pubmed ID: 29510741

Year published: 2018

Omia ID: 2141

Omia variant ID:

Turnaround information

  • 15 working days