Myasthenia gravis (MG) is an autoimmune disease. It affects the connection between the nerves and skeletal muscles. This can cause progressive muscle weakness.
The root cause of MG is unknown. It occurs when the body’s immune system attacks receptors in muscle. Normally, these receptors respond to the chemical acetylcholine (ACh). This chemical allows nerve signals to prompt the muscles to move. When the immune system prevents these receptors from working well, the muscles cannot respond to nerve signals.
The thymus is thought to play a role in some cases of MG. The thymus is an organ behind the breastbone. Immune proteins called antibodies are produced there. It is these antibodies that may target the ACh receptors. It is still not clear why the thymus begins to produce these.
|The Thymus Gland|
|Copyright © Nucleus Medical Media, Inc.|
Infants of mothers with MG are more likely to develop a temporary form. It is called neonatal MG. The mother’s abnormal antibodies enter the baby’s bloodstream. When the baby is born, there may be muscle weakness. The abnormal antibodies are often cleared from the baby in about 2 months. This will end the baby’s symptoms.
MG is most common in women less than 40 years old and in men over 60 years old. People with a family history of systemic lupus erythematosus are also at an increased risk.
Symptoms may grow more severe over time. MG may cause the following:
- Muscle weakness that increases with muscle use/exercise, and improves after resting those muscles
- Drooping eyelids
- Double and/or blurred vision
- Difficulty swallowing
- Difficulty speaking
- Difficulty walking
- Weakness of the hand muscles
- Difficulty breathing
You will be asked about your symptoms and medical history. A physical exam will be done. You will likely need to see a neurologist. This type of doctor is an expert in diseases of the nervous system. Tests may include:
- Blood tests
- Electromyography (EMG) tests—to reveal abnormalities in muscle functioning
- Repetitive nerve stimulation (a component of EMG)—may show progressively increasing muscle weakness over the course of the test
- Tensilon test—a dose of a medication called edrophonium chloride is given, which will briefly improve muscle weakness
- Pulmonary function testing to evaluate breathing an lung function
Imaging tests to see internal bodily structures may be done with:
Treatment is focused on managing MG symptoms. Talk with your doctor about the best treatment plan for you. Options may include one or more of the following:
Your doctor may prescribe the following:
- Acetylcholinesterase inhibitors
- Immunosuppressive drugs
- IV immunoglobulin therapy
Plasmapheresis is a procedure that cleans the blood of the abnormal antibodies. This process may need to be repeated at certain intervals.
Thymectomy is a surgical procedure to remove the thymus gland. Surgery may improve symptoms or bring remission in some people.
This may only be needed if breathing is severely impaired. This can happen during an episode of myasthenic crisis.
Physical and Occupational Therapy
Therapy does not generally alter the course of the disease. It may be needed to help the person cope with changes in muscle strength. It may also help with learning alternative ways to approach daily activities.
Avoiding Medications That May Worsen Symptoms
Avoid medications that may worsen MG. Some examples include:
- Certain antibiotics
- Certain medications used to treat psychiatric conditions
There are no current guidelines to prevent MG.
- EBSCO Medical Review Board Rimas Lukas, MD
- Reviewed: 09/2017
- Updated: 11/09/2015
Please note, not all procedures included in this resource library are available at Henry Ford Allegiance Health or performed by Henry Ford Allegiance Health physicians.
All EBSCO Publishing proprietary, consumer health and medical information found on this site is accredited by URAC. URAC's Health Web Site Accreditation Program requires compliance with 53 rigorous standards of quality and accountability, verified by independent audits. To send comments or feedback to our Editorial Team regarding the content please email us at HLEditorialTeam@ebscohost.com.
This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.