Myasthenia gravis
Myasthenia gravis is an autoimmune disorder that causes weakness of the skeletal muscles, often fluctuating with activity and improving with rest.
Overview
Myasthenia gravis affects the skeletal muscles used for movement. It is most commonly diagnosed in women younger than 40 and men older than 60. While uncommon in children, some infants born to affected mothers may experience temporary symptoms known as transient neonatal myasthenia gravis.
Symptoms
Weakness often begins in the eye muscles, leading to drooping eyelids (ptosis) and blurred or double vision. In ocular myasthenia, weakness is confined to the eyes, but most individuals experience broader muscle involvement, including:
- Facial and neck weakness: Unusual facial expressions, difficulty holding up the head, speech impairment (dysarthria), and chewing or swallowing problems (dysphagia).
- Limb weakness: Difficulty lifting objects, climbing stairs, or rising from a seated position.
- Respiratory distress: Weakness of the chest wall and diaphragm can lead to a myasthenic crisis, a life-threatening complication where breathing is severely impaired.
Causes
Myasthenia gravis is an autoimmune disorder where the immune system produces antibodies that attack the body's own tissues. These antibodies target proteins essential for nerve signal transmission, specifically the acetylcholine receptor (AChR) or muscle-specific kinase (MuSK). This attack reduces the signaling between nerve and muscle cells, resulting in muscle weakness.
About 75 percent of affected individuals have an abnormally large or overactive thymus gland, which may contain noncancerous tumors called thymomas. The condition is also associated with an increased risk of other autoimmune disorders, such as systemic lupus erythematosus and autoimmune thyroid disease.
Inheritance
In most cases, myasthenia gravis is not inherited. Only 3 to 5 percent of affected individuals have family members with the disorder or other autoimmune conditions, and the specific inheritance pattern remains unknown.
