Myasthenia gravis is a chronic autoimmune disorder in which the body attacks its own neuromuscular connections. This causes problems with communication between nerves and muscle, resulting in weakness. Myasthenia gravis affects the voluntary muscles of the body, especially the eyes, mouth, throat, and limbs.
In women, myasthenia gravis generally starts by age 20 to 30. In men, it usually starts after the age of 50. But this condition can occur at any age. Males are more often affected than females.
Myasthenia gravis is not inherited and it is not contagious. It generally develops later in life when antibodies in the body attack normal receptors on muscle. This blocks a chemical needed to stimulate muscle contraction.
A temporary form of myasthenia gravis may develop in the fetus when a woman with myasthenia gravis passes the antibodies to the fetus. Generally, it resolves in 2 to 3 months.
These are the most common symptoms of myasthenia gravis:
Visual problems, including drooping eyelids (ptosis) and double vision (diplopia)
Muscle weakness and fatigue. It may vary rapidly in intensity over days or even hours and worsen as muscles are used (early fatigue). For this reason, many symptoms are worse later in the day.
Facial muscle involvement causing a mask-like appearance. A smile may appear more like a snarl.
Trouble swallowing or pronouncing words
Weakness of the neck or limbs
The symptoms of myasthenia gravis may look like other health problems. Always see your healthcare provider for a diagnosis.
Flare-ups and remissions (easing of symptoms) may occur now and then during the course of myasthenia gravis. Remissions, though, are only rarely permanent or complete.
Your healthcare provider can diagnose myasthenia gravis based on your symptoms and certain tests. During the physical exam, your healthcare provider will ask about your medical history and symptoms.
A common way to diagnose myasthenia gravis is to test how you respond to certain medicines. Muscle weakness often dramatically improves for a brief time when you are given an anticholinesterase medicine. If you respond to the medicine, it supports the diagnosis of myasthenia gravis.
Other tests that may be done include:
Blood tests. These tests look for antibodies that may be present in people with myasthenia gravis.
Genetic tests. These tests are done to check for conditions like myasthenia gravis that may run in families.
Nerve conduction studies. A test called repetitive nerve stimulation may be used.
Electromyogram (EMG). This test measures the electrical activity of a muscle. An EMG can detect abnormal electrical muscle activity due to diseases and neuromuscular conditions.
Single-fiber EMG. This is a very special EMG. It records the transmission of nerve to muscle.
Treatment will depend on your symptoms, age, and general health. It will also depend on how severe the condition is.
There is no cure for myasthenia gravis. But the symptoms can often be controlled. Myasthenia gravis is a lifelong health problem. It may go into remission for extended periods. Early detection is the key to managing the condition.
The goal of treatment is to increase muscle function and prevent swallowing and breathing problems. Most people with this condition can improve their muscle strength and lead normal or near normal lives. In more severe cases, help may be needed for breathing and eating.
Treatment may include:
Medicine. Anticholinesterase medicines, steroids, or medicines that suppress the immune system’s response (immunosuppressive) medicines may be used.
Thymectomy. This is surgical removal of the thymus gland. The role of the thymus gland in myasthenia gravis is not fully understood. , People who have their thymus removed tend to need less medicine. They also tend to have fewer problems, such as needing a hospital stay, within 3 years after the surgery.
Plasmapheresis. This procedure removes abnormal antibodies from the blood and replaces the blood with normal antibodies from donated blood.
Immunoglobulin. This is a blood product that helps decrease the immune system’s attack on the nervous system. It is given intravenously (IV).
The most serious complications of myasthenia gravis is myasthenic crisis. This is a condition of extreme muscle weakness, particularly of the diaphragm and chest muscles that support breathing. Breathing may become shallow or ineffective. The airway may become blocked because of weakened throat muscles and a build up of secretions. Myasthenic crisis may be caused by a lack of medicine or by other factors, such as a respiratory infection, emotional stress, surgery, or some other type of stress. In severe crisis, a person may have to be placed on a ventilator to help with breathing until muscle strength returns with treatment.
These precautions may help to prevent or minimize the occurrence of myasthenic crisis:
Taking anticholinesterase medicines 30 to 45 minutes before meals to reduce the risk of aspiration (food entering the lung passages)
Taking anticholinesterase medicines exactly as prescribed to help maintain the strength of the breathing muscles
Staying away from crowds and contact with people with respiratory infections, such as a cold or the flu
Taking in proper nutrition to maintain optimal weight and muscle strength
Balancing periods of physical activity with periods of rest
Using stress-reduction techniques and avoiding emotional extremes
Wearing a medical alert bracelet to advise others of your condition, in case of an emergency
Tell your healthcare providers about your condition when any medicines are being prescribed. Certain medicines may interfere either with the disease or the action of the medicines you take for myasthenia gravis.
There is no cure for myasthenia gravis. But the symptoms can generally be controlled. Myasthenia gravis is a lifelong health condition. Early detection is key to managing this condition.
The goal of treatment is to increase general muscle function and prevent swallowing and breathing problems. Most people with myasthenia gravis can improve their muscle strength and lead normal or near normal lives. In more severe cases, help may be needed with breathing and eating.
Call your healthcare provider if any of these occur:
Blurred or double vision
Problems chewing and swallowing
Weakness in the arms and legs
Myasthenia gravis is a chronic autoimmune disorder in which antibodies destroy neuromuscular connections. This causes problems with communication between nerves and muscle, resulting in weakness of the skeletal muscles. It affects the voluntary muscles of the body, especially the eyes, mouth, throat, and limbs.
There is no cure for myasthenia gravis. But the symptoms can generally be controlled.
The goal of treatment is to increase general muscle function and prevent swallowing and breathing problems.
Most people with this condition can improve their muscle strength and lead normal or near normal lives.
In more severe cases, help may be needed for breathing and eating.
Tips to help you get the most from a visit to your healthcare provider:
Know the reason for your visit and what you want to happen.
Before your visit, write down questions you want answered.
Bring someone with you to help you ask questions and remember what your provider tells you.
At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you.
Know why a new medicine or treatment is prescribed, and how it will help you. Also know what the side effects are.
Ask if your condition can be treated in other ways.
Know why a test or procedure is recommended and what the results could mean.
Know what to expect if you do not take the medicine or have the test or procedure.
If you have a follow-up appointment, write down the date, time, and purpose for that visit.
Know how you can contact your provider if you have questions.
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