Myasthenia Gravis (Autoimmune Muscle Fatigue)
Myasthenia Gravis (Autoimmune Muscle Fatigue) Treatment Range
Treatment Range Hospital in Hyderabad offers expert care for Myasthenia Gravis, an autoimmune condition that causes muscle weakness and fatigue. Our skilled neurologists provide advanced treatment options including cholinesterase inhibitors to improve muscle strength and immunosuppressive therapies like steroids to control immune system flares. Recognized as one of the best hospitals in Hyderabad for Myasthenia Gravis treatment, we focus on helping patients regain mobility and quality of life.
Our comprehensive care program includes accurate diagnosis using advanced testing, personalized medication plans, and long-term monitoring to prevent relapses. For severe cases, we also provide options like plasmapheresis or IV immunoglobulin (IVIG) to manage sudden exacerbations. Each treatment is tailored to the patient’s condition and response, ensuring safe and effective management.
If you’re searching for Myasthenia Gravis treatment in Hyderabad, Treatment Range Hospital combines experienced specialists, state-of-the-art facilities, and a compassionate approach to support patients through their recovery journey and ongoing care.
- Your 6 - Phase health Process
Your Complete Myasthenia Gravis (Autoimmune Muscle Fatigue) Journey
🩺Phase 1: Symptoms Identification
- Common symptoms: Muscle weakness worsening with activity (fatigability)
- Drooping eyelids (ptosis) and double vision (diplopia)
- Difficulty speaking, chewing, or swallowing
- In severe cases, breathing difficulty (myasthenic crisis)
- Symptoms improve with rest and worsen later in the day
🔬Phase 2: OPD Consultation & Assessment
- Detailed history of symptom progression and triggers
- Neurological examination focusing on muscle strength and fatigability
- Screening for thymoma (tumor of thymus gland) with imaging
🧬 Phase 3: Causes & Risk Factors
- Autoimmune attack on acetylcholine receptors at the neuromuscular junction
- Risk factors: Female (age 20–40) or male (age 50–70), thymus abnormalities (thymoma or hyperplasia)
- Triggers for exacerbation: infections, stress, certain medications (e.g., aminoglycosides, beta-blockers)
🔍 Phase 4: Diagnosis & Investigations
- Blood tests for anti-AChR antibodies or anti-MuSK antibodies
- Electromyography (EMG) with repetitive nerve stimulation
- CT or MRI chest to check for thymoma
- Edrophonium (Tensilon) test in select cases (diagnostic challenge test)
💊 Phase 5: Treatment Plan
- Symptomatic Relief:Cholinesterase inhibitors (Pyridostigmine) to improve muscle strength
- Immunosuppressive Therapy:Corticosteroids (Prednisone)
- Long-term immunosuppressants (Azathioprine, Mycophenolate mofetil)
- In Myasthenic Crisis:Plasmapheresis or IVIG (Intravenous Immunoglobulin) for rapid symptom control
- Thymectomy if thymoma present
📅Phase 6: Recovery & Long-term Management
- Regular follow-ups to monitor medication side effects and disease progression
- Energy conservation strategies to avoid fatigue
- Vaccination and infection prevention (in immunosuppressed patients)
- Education on recognizing early signs of myasthenic crisis
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- Frequently Asked Questions
Helping you understand Our healthcare
Pyridostigmine (cholinesterase inhibitor) is first-line for symptom relief, often combined with steroids or immunosuppressants for long-term control.
There’s no permanent cure, but with treatment most patients achieve good symptom control and lead active lives.
A life-threatening worsening of weakness affecting breathing muscles. It requires immediate hospital care with IVIG or plasmapheresis.
Yes, thymectomy (removal of thymus gland) is recommended if a thymoma is present and may benefit younger patients even without a tumor.
Avoid certain antibiotics (aminoglycosides), beta-blockers, and magnesium-containing medications as they can worsen symptoms.