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Neuromyotonia, also known as Isaac's syndrome, is considered a rare neuromuscular disorder. Its exact prevalence is not well-established, but it is estimated to affect approximately 1 in 1 million individuals. The condition is characterized by continuous muscle activity and stiffness due to hyperexcitability of motor neurons, often associated with autoimmune or genetic factors. Diagnosis and management can be challenging due to its rarity and the overlap with other neuromuscular disorders.
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What is neuromyotonia?
Neuromyotonia, also known as Isaac's syndrome, is a rare disorder characterized by continuous muscle stiffness and prolonged muscle contractions. This condition is typically caused by abnormal electrical activity in the peripheral nerves, leading to muscle overactivity and stiffness. Symptoms may include muscle cramps, twitching, and difficulty relaxing muscles. Treatment options may include medications to manage symptoms and physical therapy to improve muscle function.
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