Myasthenia Gravis
Medical Review
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.



