Myasthenia Gravis

Brain & Neurology

Myasthenia gravis (MG) is an autoimmune disorder in which antibodies block the communication between nerves and muscles at the neuromuscular junction. It causes fluctuating weakness — worse with use, better with rest — of specific muscle groups (eye, face, throat, neck, limbs, breathing muscles).

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About Myasthenia Gravis

About this summary: Written by Swasthya Plus for Indian readers, using MedlinePlus, National Library of Medicine as a reference source. For personal guidance, please consult a qualified Health Expert.

Myasthenia gravis (MG) is an autoimmune disorder in which antibodies block the communication between nerves and muscles at the neuromuscular junction. It causes fluctuating weakness — worse with use, better with rest — of specific muscle groups (eye, face, throat, neck, limbs, breathing muscles). With modern treatment, most people with MG live full, active lives.

Classic features

  • Drooping eyelids (ptosis), double vision — often the first sign.
  • Weakness that worsens through the day and with repetition.
  • Slurred speech, nasal voice, difficulty chewing/swallowing.
  • Neck and limb weakness — particularly proximal (shoulder/hip).
  • Breathing difficulty in severe cases (myasthenic crisis — emergency).

Red flags — dial 112

  • Worsening breathing, swallowing, or inability to clear saliva — myasthenic crisis; ventilator support may be needed.
  • Rapidly progressive weakness.
  • Choking or aspirating food.

Diagnosis

  • Clinical examination, including fatigue tests.
  • Anti-acetylcholine receptor antibodies, anti-MuSK antibodies, anti-LRP4 — blood tests.
  • Electromyography (repetitive nerve stimulation, single-fibre EMG).
  • CT chest — for thymoma (abnormal thymus gland; present in some MG patients).
  • Rule out thyroid disease and other autoimmune conditions often associated.

Treatment

  • Cholinesterase-inhibitor tablets — symptomatic relief.
  • Steroids, steroid-sparing immunosuppressants — mainstay for disease control.
  • Intravenous immunoglobulin (IVIG), plasma exchange — for severe flares or crises.
  • Biologics and newer targeted therapies — for refractory disease; increasingly available at specialist centres in India.
  • Thymectomy — surgical removal of the thymus; indicated for thymoma; also improves outcomes in selected non-thymoma generalised MG.
  • Avoid medicines that worsen MG — some antibiotics (quinolones, aminoglycosides), magnesium sulphate, certain muscle relaxants, certain heart medicines (beta-blockers can sometimes), specific imaging contrast agents. Keep a list; carry it; tell every Health Expert about your diagnosis.

Living with MG

Pace activities; sleep adequately; treat infections and stress promptly; vaccinations (flu, pneumococcal); monitor for thyroid disease. Indian Myasthenia Gravis Association and specialist clinics provide support and information.

Reference source: MedlinePlus, National Library of Medicine