Diagnosing Myasthenia Gravis (MG)


What is myasthenia gravis?

Myasthenia gravis (MG) is a rare, lifelong autoimmune disease that involves disruption of normal communication between nerves and muscles. Nerves release a specific neurotransmitter, acetylcholine, that binds to muscle receptor sites at the neuromuscular junction of skeletal muscles. When working properly, this signals the muscles to contract. MG causes the immune system to create antibodies that block these receptor sites, resulting in communication disruption between the nerves and muscles. As fewer nerve signals are received by the muscles, muscle fatigue and weakness occur. Voluntary muscles of the body, especially the mouth, eyes, throat and limbs, are typically affected by MG.

Diagnosing myasthenia gravis

To diagnose myasthenia gravis, a physician will perform a physical examination, review medical history, and evaluate symptoms. A blood test, imaging tests, electromyography, repetitive nerve stimulation, or edrophonium test may also be performed.

Physical examination

During the physical examination, a physician will look for certain symptoms of myasthenia gravis that include, but are not limited to, the following:

  • Droopy eyelids, improper eye movement, or double vision
  • Weak grasp
  • Poor motor function
  • Reduced reflexes
  • Difficulty speaking, chewing or swallowing
  • Decreased muscle strength and tone
  • Trouble walking or poor balance
  • Improvement of droopy eyelids following a few minutes of applying an ice pack to the eyelids

Blood tests

Myasthenia gravis causes the immune system to create antibodies that block receptor sites where nerve impulses tell the muscles to contract. A blood test can check for the presence of these abnormal antibodies. Acetylcholine receptor antibodies are found in the blood of an estimated 85% of those diagnosed with MG. Muscle-specific kinase (MuSK) antibodies can also be present; however, they are only found in approximately 6% of individuals with MG. The antibody blood test is not final, since roughly about 10% of individuals with MG do not have these abnormal antibodies.

Edrophonium test

To aid in the diagnosis of myasthenia gravis, the medication edrophonium is intravenously injected. Edrophonium prevents the breakdown of acetylcholine (a neurotransmitter), which nerve cells release for muscle stimulation. A person is positive for MG if their muscles become stronger after being injected with edrophonium.

Repetitive nerve stimulation

A nerve stimulation test involves repeated stimulation of the nerves to see if the nerve’s ability to send signals to the muscle worsens when fatigued. It also checks to see how quickly the muscles tire.

Electromyography (EMG)

An electromyography (EMG) measures the electrical activity from nerves to muscles. It detects communication disruption between the nerves and muscles.


An MRI or CT scan may be performed to check the thymus gland for issues, such as a tumor or enlargement.

Did you find this helpful?
You may also like