Myasthenia Gravis
Myasthenia gravis is a chronic autoimmune disease that causes weakness in voluntary muscles by disrupting the communication between nerves and muscles.
Overview
Myasthenia gravis (MG) affects voluntary muscles, including those used for eye movement, facial expressions, talking, swallowing, and breathing. Weakness typically worsens with activity and improves with rest. It is an autoimmune disease where the immune system mistakenly attacks healthy cells.
Causes
The condition is caused by an error in nerve-to-muscle signaling. Normally, nerves release acetylcholine to trigger muscle contraction. In MG, the immune system produces antibodies that block acetylcholine from binding to muscle tissue. The thymus gland may also play a role, as it often remains large in adults with MG or may develop tumors known as thymomas.
Symptoms
- Weakness of eye muscles
- Drooping eyelids
- Blurred or double vision
- Changes in facial expressions
- Trouble swallowing
- Shortness of breath
- Speech problems
- Weakness in the arms, hands, fingers, legs, and neck
Severe weakness affecting breathing muscles is known as a myasthenic crisis, which is a life-threatening emergency.
Diagnosis & Treatment
Diagnosis involves a medical history review, physical and neurological exams, blood tests, imaging, and electromyography (EMG). While there is no cure, treatments include:
- Anticholinesterase medicines: Improve nerve-to-muscle communication.
- Immunosuppressive medicines: Decrease immune system responses.
- Monoclonal antibodies: Help reduce immune system responses.
- Plasmapheresis and intravenous immunoglobulin: Procedures to remove abnormal antibodies from the blood.
- Thymectomy: Surgical removal of the thymus gland.
Lifestyle adjustments, such as gentle exercise and healthy eating, may also be recommended.