Myasthenia Gravis (MG) is a serious neuromuscular disorder caused by the immune system mistakenly attacking receptors on muscle tissue. It leads to significant muscle weakness, especially in muscles that control the eyes and eyelids, and may also affect the jaw, limbs, and even respiratory muscles. In severe cases, MG can be life-threatening.

Common Symptoms of Myasthenia Gravis

The hallmark symptom of MG is noticeable muscle weakness that worsens as the day progresses, particularly after repeated use of the affected muscles. Early signs often include:

• Drooping eyelids (ptosis)
• Eye fatigue or blurred vision

While some individuals experience only ocular symptoms (ocular MG), others develop generalized MG, affecting multiple muscle groups. Additional symptoms may include:

• Weakness in the mouth and jaw, causing difficulty chewing, swallowing, or speaking
• Limited facial expressions
• Weakness in the arms, legs, and neck

In rare cases, a myasthenic crisis may occur—a life-threatening condition marked by severe respiratory muscle weakness, often triggered by medication changes, infections, or surgery.

 What Causes Myasthenia Gravis?

MG results from antibodies—proteins produced by the immune system—mistakenly targeting acetylcholine receptors. These receptors are essential for transmitting nerve signals that prompt muscle contraction. The most common antibodies involved are:

• Acetylcholine receptor antibodies (AChR)
• In some cases, antibodies target muscle-specific kinase (MuSK), a protein on the muscle membrane

Both types interfere with nerve-to-muscle communication, leading to progressive muscle weakness.

Why Early Detection Matters

Without timely treatment, MG can lead to severe complications such as widespread muscle paralysis and respiratory failure, significantly impacting quality of life. Recognizing symptoms early and seeking medical attention is crucial for effective management.