What is the Difference Between Myasthenia Gravis and Lambert Eaton Myasthenic Syndrome?
🆚 Go to Comparative Table 🆚Myasthenia Gravis (MG) and Lambert-Eaton Myasthenic Syndrome (LEMS) are both autoimmune disorders that affect muscle function and cause muscle weakness. However, there are key differences between the two conditions, including:
- Cause: In MG, the immune system targets the acetylcholine receptor on the nerve, while in LEMS, the immune system targets the voltage-gated calcium channel on the nerve.
- Symptoms: While both conditions share similar symptoms, such as muscle weakness and fatigue, there are some differences. Eye muscle weakness in LEMS is usually milder and is never the first or only symptom. In contrast, MG often starts with muscle weakness in the upper legs for only 12% of people, and severe weakness in the breathing muscles is less common with LEMS than with MG.
- Onset and Progression: Both MG and LEMS are chronic autoimmune disorders, but they may present differently and affect different muscle groups.
- Diagnosis: Diagnostic criteria and tests may vary between the two conditions, as they target different parts of the neuromuscular junction.
- Treatment: Although both conditions may involve similar treatments, such as immunosuppressive medications and therapies to improve neuromuscular communication, specific treatments may differ based on the underlying cause and severity of the condition.
Understanding the key differences between MG and LEMS can help patients and healthcare providers make informed decisions about diagnosis and treatment.
Comparative Table: Myasthenia Gravis vs Lambert Eaton Myasthenic Syndrome
Myasthenia Gravis (MG) and Lambert-Eaton Myasthenic Syndrome (LEMS) are both autoimmune neuromuscular disorders that cause muscle weakness. They share similarities in symptoms but differ in causes, risk factors, onset and progression, diagnosis, and treatment, as well as the populations they predominantly affect. Here is a table summarizing the differences between the two conditions:
Feature | Myasthenia Gravis (MG) | Lambert-Eaton Myasthenic Syndrome (LEMS) |
---|---|---|
Typical First Symptom | Diplopia (double vision) | Difficulty arising from bed or chair |
Autonomic Symptom | None | Dry mouth |
Weakest Muscles | Extraocular (eye muscles) | Proximal leg muscles |
Deep Tendon Reflexes | Normal | Decreased |
Autoantibody Target | Postsynaptic acetylcholine receptor | Presynaptic voltage-gated calcium channel |
Diagnostic Test | Repetitive nerve stimulation with <60% decrease in muscle action potential | High-frequency repetitive nerve stimulation with >60% increase in muscle action potential |
Associated Cancer | 10% to 20% of cases, more common in women and after 40 years of age | 25% to 35% of cases, especially in middle-aged adults with small lung cancer and a history of smoking |
MG is more prevalent in young women in their 20s or 30s and older men in their 60s or 70s, while LEMS is more common in middle-aged adults, particularly those with small lung cancer and a history of smoking.
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