Dystonia is not a new condition. It affects thousands of people every year. Contrary to popular belief, dystonia is not a normal consequence of growing older. As a matter of fact, the onset of dystonia can be at any age. Dystonia is not a discriminatory condition, as it will affect men, women or children.
Presentation of dystonia may be varied. Classically, dystonia is defined as a movement disorder, which can affect any part of the body. The abnormal movement can be focal, such as twitching of an eyelid, or global, which could include the arm and hand, a leg, or even the entire upper torso. A dystonic movement disorder can also include abnormal muscle tone, twitching, or an unusual angulation of a joint. There are certain characteristic movement patterns that are specific and diagnostic to certain regions of the brain. Depending on the area of the brain involved with the tremor, different symptoms may be apparent.
There are three primary types of dystonia: basal ganglionic, mesolimbic, and dystonia from the cerebellum. All three types are from the brain or brainstem, but presentation can be clinically different with symptoms.
Historically, treatment for dystonia has been surgery, drug therapy and/or botulinum toxin A injections into the affected muscle. Botulin toxin paralyzes the muscle tissue temporarily. It does not fix the original cause of the dystonia. At best, the effectiveness of the botulinum toxin A is three to four months. At this time, the body develops an auto-immune response to treatments, therefore the effectiveness of the injections is diminished. And until recently, this was the only effective treatment.
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