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Myasthenia gravis is a chronic autoimmune neuromuscular illness that produces weakening in the skeletal muscles, which worsens during periods of activity and improves when in rest.
- These muscles are responsible for the functions of breathing and moving bodily parts, including the arms and legs.
- Myasthenia gravis is of Latin and Greek origin, and its term means "grave or severe muscle weakness."
- The majority of cases of myasthenia gravis are not as extremely critical, despite the fact that there is no known cure.
- Symptoms can typically be managed with the help of available medicines, allowing patients to enjoy a high quality of life.
- The life expectancy of the majority of affected persons is average.
Read More: Tumor
Key terms: Autoimmune Diseases, Nicotinic Acetylcholine Receptors, Myasthenia gravis, Muscles, Neuromuscular, Thymus
Myasthenia Gravis Definition
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Myasthenia Gravis can be defined:
| “A condition which causes abnormal weakness of certain muscles.” |
- It is a rare chronic autoimmune disease marked by muscular weakness.
- It includes the circulation of antibodies which causes nicotinic acetylcholine receptors to be blocked at the postsynaptic neuromuscular joint.
Read Also:
| Topic Related Concepts | ||
|---|---|---|
| Pituitary Gland | Blood Cancer | Genetics |
| White blood cells | Carcinogenicity and Toxicity | Heart |
Types of Myasthenia Gravis
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There are basically several types of Myasthenia Gravis and few of them are as given below:
Congenital Myasthenia Gravis
Congenital Myasthenia Gravis can be stated as a condition in which muscle weakness gets worsened with physical exertion.
- It is basically inherited. It can be inherited from both the parents that are involved in nerve- muscle communication.
- It is estimated to occur in 2-12 people per million.
Ocular Myasthenia Gravis
Ocular Myasthenia Gravis is explained as a condition in which the muscles that move eyes and eyelids get affected. It is estimated to occur in 1/5000.
Generalized Myasthenia Gravis
Generalized Myasthenia Gravis is defined as a condition in which multiple muscle groups are affected throughout the body
- It is also called Generalized Myasthenia Gravis.
- It is estimated to occur in 14-40 per million.
Transient Neonatal Myasthenia Gravis
Transient Neonatal Myasthenia Gravis can be defined as a postsynaptic neuromuscular transmission defect. It is found in study that 21% of the infants born are acquired with Transient Neonatal Myasthenia Gravis.
Juvenile Myasthenia Gravis
Juvenile Myasthenia Gravis is stated as a situation in which an autoimmune disorder of the neuromuscular junction results in ocular manifestations or generalized weakness, with onset before 18 years of age. It is estimated to occur in 1 per million or 2 per million.
Read Also: Genetic Disorders
Symptoms of Myasthenia Gravis
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Muscle weakness caused by Myasthenia Gravis worsens as the affected muscle is used. The symptoms of this condition also improve with rest. Moreover, the symptoms progresses with respect to time since the onset of the disease.
- The primary symptom of Myasthenia Gravis is the weakening of voluntary skeletal muscles which control muscles in specific areas.
- The muscles so weakened fail to contract as they become unresponsive to impulse.
The most common myasthenia gravis signs and symptoms that can be seen are:
Eye muscles
More than 50% of the people who suffer from Myasthenia Gravis first see the eye muscle symptom.
- In this one or both the eyelids droop. This is called Ptosis.
- The person faces double vision or diplopia and this can be horizontal or vertical.
- Diplopia can be improved or resolved by closing one eye.
![Drooping of eyelids due to Myasthenia Gravis]()
Drooping of eyelids due to Myasthenia Gravis
Read Also: Saliva: Roles, Importance & Digestion of Food
Face and Throat Muscles
The face and throat muscle symptom is faced by almost 15% of the people suffering from Myasthenia Gravis.
- In this the speaking is impaired. Your speech may sound nasal.
- One can face difficulty in swallowing. You might get choked and cannot drink properly.
- Trouble during chewing. The muscle used for chewing gets tired half a way.
- Change in facial expression. This condition also affects simple facial movements such as, smiling.
![Facial expression due to Myasthenia Gravis]()
Facial expression due to Myasthenia Gravis
Neck and Limb muscles
Myasthenia Gravis causes weakness in the neck, arms, and legs.
- Weakening in leg muscles impairs walking.
- Weak neck muscles make it hard to hold the head in proper position.
![Weak neck muscle due to Myasthenia Gravis]()
Weak neck muscle due to Myasthenia Gravis
Read Also:
| Topic Related Concepts | ||
|---|---|---|
| Pituitary Gland | Blood Cancer | Genetics |
| White blood cells | Carcinogenicity and Toxicity | Heart |
Causes of Myasthenia Gravis
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The primary cause for Myasthenia Gravis is when there is improper communication between nerves and a muscle which is interrupted by a neuromuscular joint.
- The other leading myasthenia gravis cause is that the neuromuscular joint is affected with acetylcholine which causes muscle contraction that no longer produces contractions required in muscle movement.
- Antibodies too can block the function of a protein called muscle-specific receptor tyrosine kinase, sometimes referred to as Musk.
- The thymus gland which is situated in the upper chest and beneath the breastbone triggers or maintains the production of the antibodies that block acetylcholine.
Myasthenia Gravis Complications
Some of the Complications of Myasthenia Gravis include:
- a) Myasthenic crisis:
- Myasthenic crisis is a life threatening condition in which the muscles controlling respiration become too weak to work.
- In such cases emergency breathing treatment is assisted to the patient.
- b) Thymus gland tumors:
- Some people get tumors in the thymus gland, a gland which is involved in a healthy immune system.
- Most of the tumors called thymomas are not cancerous but can lead to low immune system.
Myasthenia Gravis Diagnosis
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As we have understood the myasthenia gravis meaning, we should understand how such a condition can be diagnosed.
- This is a long term auto immune condition which results in muscular weakness. And may get worse on improper treatment.
- The first test for diagnosis is a blood test which tests for antibodies, which acts as a barrier for communication between muscles and nerve cells. High antibodies indicate the condition is present.
- The second test is a nerve test and done after a blood test is found negative. The test consists of needles inserted in the eyes or forehead and the test is known as electromyography. The electrical recordings indicate whether the condition is present or not.
- A CT scan or MRI scan of the chest helps to assess the size of the thymus. An edrophonium test may also be done.
Treatment Of Myasthenia Gravis
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There is no particular cure for Myasthenia Gravis, but treatment can help relieve signs and symptoms. Though this disease can affect people of any age, it's more common in women younger than 40 and in men older than 60. But it does have treatments like medication and therapy.
- As it is caused by the malfunction of the immune system and attacks body tissues and hence is a non-curable disease.
- The treatment is to deal with symptoms and control activity of the immune system.
- Medications include cholinesterase inhibitors, corticosteroids and immunosuppression that help to control the symptoms of the condition and bring them into manageable proportions.
- Intravenous therapy helps in treating the condition in the short term or before conducting surgery or any therapy.
- Another treatment is surgery of a tumor in the thymus gland. A thymectomy is done through open surgery and minimally invasive therapy.
Read Also:
| Chapter Related Topics | ||
|---|---|---|
| Sliding Filament Theory | Deltoid Muscles | Tissue Culture |
| Central nervous system | Types of Joints | Pelvic Bones |
Things to Remember
- Myasthenia gravis was first recognized by Thomas Willis, a 17th century Oxford physician.
- Myasthenia Gravis is a form of autoimmune disease.
- In Myasthenia Gravis, there is low activity or even over activity of the immune system which leads the body to attack and damage its tissues.
- Myasthenia Gravis occurs at any age but can be seen often at the age of 20-40 in women and 50-80 in men.
- The Myasthenia Gravis symptoms include drooping of eyelids, neck is not held in position due to weak neck muscles, and impaired walking etc.
- In myasthenia gravis, your immune system attacks a receptor in your muscles and the signals to move the muscle can’t get through.
Read More: Immunity
Previous Year Questions
- Stimulation of a muscle fiber by a motor neuron occurs at….[NEET 2014]
- In human body which one of the following is an atomically correct ?...[NEET 2007]
- A deltoid ridge occurs in...[NEET 1990]
- Number of cervical vertebrae in camel is...[NEET 1990]
- Calcium is important in skeletal muscle contraction because it...[NEET 2018]
- Colle's fracture is associated with...[BHU UET 2009]
- Which one of the following items gives its correct total number?...[NEET 2008]
- ATPase enzyme needed for muscle contraction is located in -[NEET 2004]
- Inter-articulated disc is found in...[BHU UET 2005]
Sample Questions
Ques. What is Myasthenia gravis? (2 mark)
Ans: Myasthenia gravis is defined as an Auto-immune disorder affecting neuromuscular junction leading to fatigue, weakening and paralysis of skeletal muscle. It is a rare chronic autoimmune disease marked by muscular weakness and also it includes the circulation of antibodies which causes nicotinic acetylcholine receptors to be blocked at the postsynaptic neuromuscular joint.
Ques.What is Thymectomy? (1 mark)
Ans: Thymectomy is known as the resection of the thymus gland. It is typically performed on patients who suffer from myasthenia gravis and thymoma.
Ques. State a few treatments to delay progression of Myasthenia Gravis? (2 marks)
Ans: Well there is no particular cure for Myasthenia Gravis, but treatment can help relieve signs and symptoms.
- The treatment is to deal with symptoms and control activity of the immune system.
- Medications include cholinesterase inhibitors, corticosteroids and immunosuppression that help to control the symptoms of the condition and bring them into manageable proportions.
- Intravenous therapy helps in treating the condition in the short term or before conducting surgery or any therapy.
- Another treatment is surgery of a tumor in the thymus gland. A thymectomy is done through open surgery and minimally invasive therapy.
Ques. What is Juvenile Myasthenia Gravis? (1 mark)
Ans: Juvenile Myasthenia Gravis is stated as a situation in which an autoimmune disorder of the neuromuscular junction results in ocular manifestations or generalized weakness, with onset before 18 years of age. It is estimated to occur in 1 per million or 2 per million.
Ques. What is the prognosis of Myasthenia Gravis? (3 marks)
Ans: Although MG cannot be cured, it can be treated. Many individuals with MG can lead very typical lives.
Typically, the first one to three years are the most challenging, as this is when numerous symptoms manifest. It can take time to experiment with several therapies to see which one is most effective.
MG is referred to as the "snowflake disease" since its symptoms vary from patient to patient. Periods of remission characterized by the absence of symptoms are a possibility. However, it is impossible to anticipate if remission will occur or how long it will remain.
Ques. Can Myasthenia Gravis inherited? (2 marks)
Ans: MG is not often considered a hereditary disease. However, it is not uncommon for additional family members to have an autoimmune disease if one person has one. A mother is able to transmit a transient form of MG to her newborn kid. Infrequently, the disease can affect numerous family members.
Ques. What is a thymoma? (2 marks)
Ans: Some patients who have MG end up developing tumors on their thymus gland, which are referred to as "thymomas." In most situations, thymomas do not progress to cancer, but this is not always the case. Thymomas can, on occasion, become cancerous. Once a thymoma has been identified, surgical removal of the growth is the recommended next step in treatment.
Ques. What makes MG worse? (2 marks)
Ans: The MG or Myasthenia Gravis symptoms may become temporarily more severe if you are exposed to the following: stress, lack of sleep, illness, overexertion, pain, extreme heat or cold (including the weather outside, hot showers or baths, saunas, hot tubs, hot foods or beverages), certain chemicals, or a combination of these factors (for instance, in insecticides and lawn treatments).
Ques. What symptoms are not expected in patients with myasthenia gravis? (2 marks)
Ans: Patients diagnosed with myasthenia gravis are not likely to exhibit the symptoms of memory loss, urine incontinence, numbness, a lack of sensation, or incoordination. These symptoms are not typical of the condition. If they are real, then we need to look into other possible explanations.
Ques. State a few types of Myasthenia gravis and explain in brief. (5 marks)
Ans: There are several types of Myasthenia gravis but few of them are as follows:
1) Congenital Myasthenia Gravis:
Congenital Myasthenia Gravis is a condition where muscle weakness worsens with physical exertion. It is estimated to occur in almost 2-12 per million people.
2) Ocular Myasthenia Gravis:
Ocular Myasthenia Gravis is where the muscles of the eyes and eyelids get affected. It is estimated to occur in 1/5000.
3) Generalized Myasthenia Gravis:
Generalized Myasthenia Gravis occurs when multiple muscle groups are affected throughout the body. It is estimated to occur in 14-40 per million.
4) Transient Neonatal Myasthenia Gravis:
Transient Neonatal Myasthenia Gravis is a condition wherein postsynaptic neuromuscular transmission defect is found. It is found in study that 21% of the infants
5) Juvenile Myasthenia Gravis:
Juvenile Myasthenia Gravis is an autoimmune disorder of the neuromuscular junction that leads to ocular or generalized weakness. It occurs befor 18 years of age. It is estimated to occur in 1 per million or 2 per million.
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