Myasthenia Gravis

Myasthenia Gravis (MG) is an autoimmune condition that causes signal transmission issues at the neuromuscular junction. As a result, the muscles get fatigue fast and improve after taking rest.

It mostly affects the muscles that regulate eye movements, facial expressions, chewing, and swallowing in the early stages. As the condition worsens, the neck and limb muscles may be affected, making it difficult to hold the head up, walk upstairs, and raise the arms. Breathlessness may occur if left untreated.

Although this condition does not run in families, those who develop autoimmune conditions are more likely to develop myasthenia gravis.


The following are the types of myasthenia gravis:

  • Ocular myasthenia gravis
  • Juvenile myasthenia gravis
  • Congenital myasthenia gravis
  • Transient neonatal myasthenia gravis
  • Generalized myasthenia gravis
Myasthenia Gravis


Initially patients may notice drooping of eyelids and impaired or double vision. Patients may present with difficulty in swallowing and chewing . Generalised weakness usually develops in first 2 years of illness. Myasthenia gravis symptoms, in general, include:

In severe MG conditions the respiratory muscles become so weak that one can't control them. This is a medical emergency that requires the use of a ventilator to assist patients in breathing. Around 15% to 20% of people with myasthenia gravis will have at least one myasthenic crisis. It can be caused by an infection, stress, surgery, or a medical reaction.

When to see a doctor?

If you experience drooping of eyelids ,double vision or chewing difficulty which worsens by evening , it could be a symptom of myasthenia so consult a neurologist or a rheumatologist.


Myasthenia gravis is not hereditary or contagious. It usually appears later in life when antibodies in the body assault normal muscle receptors. This inhibits a hormone that is required to induce muscular contraction. When a mother with myasthenia gravis transfers the antibodies to the baby, a short form of myasthenia gravis might emerge. It usually resolves itself in 2 to 3 months.

Risk Factors

Muscular dystrophy is a hereditary disease. A family history of muscular dystrophy puts you at risk of being a carrier or getting the disease.

  • Smoking and tobacco chewing
  • Physical inactivity
  • Obesity
  • Insufficient diet including lower rate of fish consumption.


Myasthenia gravis complications are curable; however, some can be fatal.

Myasthenic crisis

Myasthenic crisis occurs when the respiratory muscles that control breathing become too weak to function. Emergency care and mechanical breathing support are required. Medications and blood-filtering therapy or Immunoglobulin therapy enable people to breathe normally again.

Thymus gland tumours

Some patients with myasthenia gravis develop thymus gland tumours, a gland beneath the breastbone linked with the immune system. Most of these tumours, known as thymomas, are not cancerous (malignant).

Other disorders

Myasthenia gravis patients are more likely to have the following conditions

Autoimmune conditions

Myasthenia gravis patients may be prone to autoimmune diseases such as rheumatoid arthritis or lupus.

Underactive or overactive thyroid

The thyroid gland, which is located in the neck, secretes hormones that control metabolism. If the thyroid is underactive (hypothyroidism), people may struggle with colds, weight gain, and other concerns. An overactive thyroid (hyperthyroidism) can create problems with heat, weight loss, and other complications.


It is difficult to avoid MG; however, people can take steps to stop a flare-up of symptoms or prevent consequences from developing. These include practising good hygiene to avoid infections and promptly treating them if they develop. It is a good idea to avoid extreme heat and overexertion. Effective stress management can also lower the frequency and severity of symptoms.


Myasthenia gravis can be diagnosed based on the symptoms and certain tests. The doctor will inquire about the medical history and symptoms throughout the physical examination.

Edrophonium test

The doctor will give an injection of edrophonium chloride to see if it improves muscle strength. If it happens, it might be an indication of myasthenia gravis.

Ice pack test

If you have a drooping eyelid, the doctor may place an ice pack on it for 2 minutes to examine if the cold sensation affects it.

Blood test:

Routine blood tests to rule out other causes. Achr and musk autoantibodies are to be tested.

Repetitive nerve stimulation

This test sends small electrical pulses through electrodes into the muscles to examine if your nerves respond to the impulses.

Imaging test

The doctor may recommend a CT scan or an MRI to look for a tumour on the thymus area.

Pulmonary functioning tests:

The doctor will examine the breathing ability to check if myasthenia gravis has affected the lungs.


MG is a treatable condition; with treatment, many patients may live normal lives. Treatment options include


Anticholinesterase medications, steroids, or medications that may be used to suppress the immune system's reaction (immunosuppressive).


The thymus gland is surgically removed in all patients with myasthenia who has hyperplasia or neoplasm of thymus.


A technique in which abnormal antibodies are removed from the blood and replaced with normal antibodies from donor blood.


It is a blood product that helps to reduce the immune system's attack on the neurological system. It is administered intravenously (IV).
Both are useful in patients who are in myasthenia crisis

Dos and Don’ts

Most of the medications will have an effect on nerve muscle junction and can worsen myasthenia ,so consult a Neurophysician before starting any new medications.

The key to managing this condition is early diagnosis. The goal of treatment is to improve overall muscular function while preventing swallowing and breathing problems. Most patients with myasthenia gravis can restore their muscle functions and live normal or near-normal lives.

Adopt a positive attitude and remain cheerfulGet exposed to extreme heat
Maintain good hygieneEat dry and hard foods that can easily crumble and get stuck into the windpipe.
Make regular visits to your doctorDrink alcohol and smoke
Take adequate rest.Drink less water
Avoid stressLead a sedentary lifestyle

These dos and don'ts can assist people manage the condition by avoiding and reducing its negative effects. Make and keep regular follow-up appointments with the doctor to keep track of the symptoms and to control the severity of the disease.

Myasthenia Gravis Care at Medicover Hospitals

At Medicover hospitals, we have the best team of rheumatologists and neurologists who work together to provide myasthenia gravis treatment with utmost precision. Our highly skilled team utilises the latest medical equipment, diagnostic procedures and technologies to treat various autoimmune diseases and ailments. For myasthenia gravis, we adopt a multi-disciplinary approach to provide comprehensive care to the patients and attend to all their medical needs for faster and sustained recovery.


Make an appointment just in few minutes - Call Us Now