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What is Lambert-Eaton Myasthenic syndrome?

Lambert-Eaton myasthenic syndrome (LEMS) is an uncommon neuromuscular disorder characterized by weakness in muscles of the upper arms and upper legs, and less commonly, muscles of the neck, speech, swallowing, breathing and eye movement. LEMS is an autoimmune disease, referring to the fact that antibodies are produced by the body against its own tissues. The frequency of LEMS is less than one in every 1,000,000 people. The disorder is not hereditary. Lambert-Eaton myasthenic syndrome (LEMS) is associated in 40% of cases with cancer, most often with small cell cancer of the lung and less often with other tumors. The neuromuscular defect in LEMS is due to insufficient release of the neurotransmitter acetylcholine by nerve cells.

More information on Lambert-Eaton Myasthenic syndrome

What is Lambert-Eaton Myasthenic syndrome? - Lambert-Eaton myasthenic syndrome (LEMS) is an uncommon neuromuscular disorder characterized by weakness in muscles of the upper arms and upper legs.
What causes Lambert-Eaton Myasthenic syndrome? - Lambert-Eaton myasthenic syndrome (LEMS) is caused by a disruption of electrical impulses between these nerve and muscle cells.
What're the symptoms of Lambert-Eaton Myasthenic syndrome? - The symptoms of Lambert-Eaton Myasthenic syndrome include muscle weakness, a tingling sensation in the affected areas, fatigue, and dry mouth.
How is Lambert-Eaton Myasthenic syndrome diagnosed? - The diagnosis of Lambert-Eaton Myasthenic syndrome is based on a typical history with in addition with low compound muscle action potential.
What's the treatment for Lambert-Eaton Myasthenic syndrome? - Multiple treatment options are available to improve symptoms and sometimes of Lambert-Eaton Myasthenic syndrome and produce remission.
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