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Is there any treatment?
Most people with myotonia congenita don’t require special treatments. Stiff muscles usually resolve with exercise, or light movement, especially after resting. For individuals whose symptoms are more limiting, doctors have had some success with medications such as quinine, or anticonvulsant
drugs such as phenytoin. Physical therapy and other rehabilitative therapies are also sometimes used to improve muscle function.
What is the prognosis?
Most individuals with myotonia congenita lead long, productive lives. Although muscle stiffness may interfere with walking, grasping, chewing, and swallowing, it is usually relieved with exercise.
What research is being done?
The National Institute of Neurological Disorders and Stroke (NINDS) conducts research related to myotonia congenita in its
clinics and laboratories at the National Institutes of Health (NIH), and also supports additional research through grants
to major medical institutions across the country. Current research is exploring how, at the molecular level, the defective gene in myotonia congenita causes the specific symptoms
of the disorder. Additional research is focused on developing animal models of the disorder to test potential treatments and therapies.
Synonyms: Thomsen's Myotonia,Becker's Myotonia