What is Myasthenia Gravis?
Myasthenia Gravis is a chronic autoimmune neuromuscular disorder that causes weakness of voluntary muscles, which are responsible for actions such as talking, chewing, breathing, and walking. The hallmark feature of this condition is muscle weakness that worsens with activity and improves with rest.
Causes
Myasthenia Gravis occurs when the body’s immune system produces antibodies that block or destroy acetylcholine receptors at the neuromuscular junction—the site where nerves communicate with muscles. This disruption prevents proper signal transmission, resulting in weak muscle contractions.
Common Symptoms
Symptoms may vary in severity but commonly include:
Symptoms often worsen as the day progresses or with repeated muscle use and improve after rest. In severe cases, weakness of the respiratory muscles can lead to a myasthenic crisis, which is a medical emergency requiring immediate treatment.
Who is Affected?
Myasthenia Gravis can affect individuals of any age but is more commonly seen in:
Diagnosis
Diagnosis of Myasthenia Gravis is based on the following investigations:
Treatment
Prognosis
With appropriate treatment and lifestyle modifications, many individuals with Myasthenia Gravis are able to live full and active lives. Avoiding stress, infections, and excessive physical exertion can help reduce symptom flare-ups. Regular follow-up with a neurologist is essential to monitor disease progression and optimize treatment.
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