Myasthenia Gravis

Medical Review

Written by: Dr. Von Chiao Wen Doctor of Medicine (MD), N.I. Pirogov Russian National Research Medical University
Reviewed by: Dr. Lee Chin Meng Doctor of Medicine (MD), Manipal Academy of Higher Education (MAHE)

Overview of Myasthenia Gravis

Myasthenia Gravis is an autoimmune disease mediated by autoantibodies to nicotinic acetylcholine receptors on the post-synaptic side of the neuromuscular junction. It affects the voluntary muscles and characterised by weakness and fatigability.

Signs and Symptoms of Myasthenia Gravis

Muscle weakness, Fatigue, Diplopia (double vision), Ptosis, Difficulty chewing, Difficulty swallowing, Proximal myopathy, Mushy or nasal quality speech, Facial weakness

Common Causes of Myasthenia Gravis

Autoantibody

Risk Factors of Myasthenia Gravis

Presence of autoimmune disease, Age less than 50 years in female and more than 50 years in male, Thymic hyperplasia or atrophy or tumour

Investigation Techniques for Myasthenia Gravis

Acetylcholine receptor antibody test, Tensilon test, Electromyography (EMG), CT scan to exclude thymoma

Treatment and Prevention of Myasthenia Gravis

Anticholinesterase, Immunosuppressive therapy, Thymomectomy

Available Myasthenia Gravis Medicines

No medicines currently available for this condition.

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