Myasthenia gravis is an autoimmune disease characterized by fluctuating weakness of skeletal muscles. It results from antibodies formed against acetylcholine receptors at the neuromuscular junction, reducing acetylcholine levels and impairing muscle contraction. Clinical manifestations include easy fatigability of muscles involved in eye movement, facial expression, chewing, swallowing, and breathing. Diagnostic tests include Tensilon testing which shows improved muscle contractility after administration of an anticholinesterase agent. Treatment focuses on anticholinesterase medications, corticosteroids, and plasmapheresis to remove acetylcholine antibodies.