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Myasthenia Gravis is an autoimmune neuromuscular disorder causing weakness in voluntary muscles due to autoantibodies against acetylcholine receptors and thymus gland abnormalities. Key clinical features include ptosis, diplopia, and muscle weakness that worsens with activity, while diagnosis involves tests like the Edrophonium test and EMG. Management includes anticholinesterase drugs, corticosteroids, thymectomy, and nursing care focused on respiratory monitoring and patient education.

Author

shivam bajaj

Language

EN