Dyskinesias (Paroxysmal)

Description

Paroxysmal dyskinesias are neurologic conditions characterized by sudden episodes of abnormal involuntary movements (hyperkinesias). These may include any combination of involuntary, rapid, randomly irregular jerky movements (chorea); relatively slow, writhing motions that appear to flow into one another (athetosis); increased muscle tone with repetitive, twisting, patterned movements and distorted posturing (dystonia); and uncontrollable flinging movements of an arm, a leg, or both (ballismus). The term paroxysmal indicates that the abnormal movements are sudden and unpredictable, with a relatively rapid return to normal motor function and behavior.

Paroxysmal dyskinesias are often classified into paroxysmal kinesigenic dyskinesia (PKD) and paroxysmal non-kinesigenic dyskinesia (PNKD), based upon precipitating factors that precede or trigger the episodes of abnormal, involuntary movement. In patients with PKD the episodes of hyperkinetic movements are provoked by sudden voluntary movement or unexpected stimuli (startle). In contrast, in those with non-kinesigenic dyskinesia, the attacks may occur spontaneously while at rest or out of a background of normal motor activity, but may be exacerbated by alcohol or caffeine consumption, stress, fatigue, or other factors. Other types of paroxysmal dyskinesias include episodes precipitated by prolonged exertion (paroxysmal exertion-induced dyskinesia) or sleep (paroxysmal hypnogenic dyskinesia).

Paroxysmal dyskinesias may also be further categorized according to the duration of the attacks. They may be described as "short-lasting" if episodes are less than or equal to 5 minutes or "long-lasting" if attacks are longer than 5 minutes. The paroxysmal dyskinesias may be familial, appear to occur randomly for unknown reasons (sporadically), or occur secondary to other underlying conditions (symptomatic).

Please see the following topics related to paroxysmal dyskinesias below, and available on the left side of this page.

• Clinical Features and Classification
• Genetics
• Etiology of Secondary Paroxysmal Dyskinesias
• Pathophysiology
• Epidemiology
• Diagnosis
• Treatment
• Additional Resources
• References