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Neurology

Myasthenia Gravis Treatment

Expert myasthenia gravis diagnosis and immunotherapy by Dr. Bharath Kumar Surisetti. Acetylcholine receptor antibody testing and personalised treatment in Hyderabad.

80+MG Cases
9+Years Exp.
BiologicAccess
Myasthenia Gravis Treatment

Overview

Myasthenia Gravis (MG) is an autoimmune neuromuscular junction disorder where antibodies (AChR or MuSK) block the acetylcholine receptor, causing fatigable muscle weakness particularly affecting the eyes, face, swallowing and limbs.

Dr. Bharath Kumar Surisetti diagnoses MG through antibody testing, repetitive nerve stimulation and single-fibre EMG, then manages the condition with acetylcholinesterase inhibitors, immunosuppressants and biologic therapies for refractory disease.

Symptoms & Conditions We Treat

Ptosis and Diplopia

Drooping eyelid and double vision - earliest and most common symptoms

Fatigable Weakness

Weakness that worsens with activity and improves with rest

Dysarthria and Dysphagia

Slurred speech and swallowing difficulty in bulbar MG

Myasthenic Crisis

Respiratory failure from diaphragm weakness - a medical emergency

Limb Weakness

Proximal limb weakness making arm raising or climbing stairs difficult

Cholinergic Crisis

Over-medication crisis with increased secretions and muscle fasciculations

Our Treatment Approach

1

Antibody Testing

AChR and MuSK antibody titres; seronegative cases may need single-fibre EMG.

2

Repetitive Nerve Stimulation

Decremental response on 3Hz stimulation confirming neuromuscular junction defect.

3

CT Chest for Thymoma

All MG patients screened for thymoma with CT chest; thymectomy may be curative.

4

Individualised Immunotherapy

Pyridostigmine plus immunosuppression; biologics (eculizumab, efgartigimod) for refractory cases.

Treatment Options

Symptomatic Treatment

  • Pyridostigmine (Mestinon)
  • Dose titration
  • Managing cholinergic side effects
  • Crisis prevention

Immunosuppression

  • Prednisolone
  • Azathioprine
  • Mycophenolate mofetil
  • Methotrexate

Acute Treatment

  • IVIG for exacerbation
  • Therapeutic plasma exchange
  • ICU support for crisis
  • Respiratory monitoring

Biologic Therapies

  • Eculizumab (Soliris)
  • Efgartigimod (Vyvgart)
  • Ravulizumab
  • Rituximab for MuSK-MG

Why Choose Srilekha's Clinic?

Expert Neurologist

DM-qualified neurologist with 9+ years and 2000+ patients treated

Advanced Diagnostics

MRI, EEG, NCS/EMG and comprehensive neurological workup

Personalised Care

Treatment plans tailored to your condition and lifestyle

Evidence-Based

Latest international neurology guidelines followed strictly

Prompt Treatment

No unnecessary delays - urgent cases seen on priority

Long-Term Support

Ongoing management and monitoring for chronic conditions

Neurology FAQ

Frequently Asked Questions

Quick answers about this condition. Can't find what you need? Chat with us directly.

MG is an autoimmune neuromuscular disease causing fatigable weakness — weakness that worsens with use and improves with rest. It commonly affects eyes, face, swallowing, and limb muscles.

Most common: drooping eyelid (ptosis), double vision (diplopia), difficulty swallowing, and slurred speech.

Diagnosis includes AChR/anti-MuSK antibodies, repetitive nerve stimulation, single-fibre EMG (most sensitive), and CT chest to look for thymoma.

A crisis involves severe respiratory muscle weakness requiring ICU care. Triggers: infections, surgery, or medication changes. It is a medical emergency.

Pyridostigmine (symptomatic), prednisolone, azathioprine, IVIG/plasmapheresis for crises, and thymectomy in AChR-positive patients with or without thymoma.

Book via WhatsApp +91 9963 138 139. Dr. Bharath Kumar at Habsiguda, Hyderabad.