Introduction: It is an autoimmune disease that leads to fluctuating muscle weakness and fating that worsens with exercise and improves with rest. It is caused by a disruption in nerve and muscle communication. The far more prevalent muscle fibre disease involving the motor neuron is myasthenia gravis (MG) (NMJ). A variable weakness that worsens in the afternoon is the most common symptom. Eye, throat, and extremity muscles are frequently engaged. The transmission of electrical impulses across the neuromuscular junction is reduced due to the formation of autoantibody against particular postsynaptic membrane proteins, causing muscle weakness. Infections, vaccinations, surgeries, and medications are just a handful of the possible causes of MG. Main symptoms and clinical findings: A female 36 old admitted to AVBRH Hospital chief complete is difficult in swallowing, slurred or nasal speech, difficulty chewing, and facial neck and extremityweaknessoccur, which is primarily Asymmetrical, significantly affected of intraocularbulbar is more rare cases. The primary diagnosis and therapeutic interventions, and outcomes: A female 36 old admitted to AVBRH Hospital with chief complete have difficulty swallowing, facial neck and extremityweakness, proximal limb or truncal musculature diplopia due to the involuntary extrinsic ocular muscle.IV fluidattaché. Advice to check the vital sing sand maintains the record and observation of the patient.She came for treatment, and her treatment started when admitted injectable pan 40 mg, antibiotics ampicillin 250 mg, tension ((edrophonium), an anticholinesterase.As per the patient, treatment is ongoing, and the patient's prognosis is better. Conclusion: Myasthenia Gravis is a complex disorder with various visible and subtle signs and symptoms. The presence of ptosis and diplopic should prompt the practitioner to perform an MG work-up.

Myasthenia Gravis, Neurons,