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Paroxysmal kinesigenic dyskinesia is diagnosed using a strict set of guidelines.
Mutations in this gene are associated with paroxysmal kinesigenic dyskinesia.
Paroxysmal kinesigenic dyskinesia has been shown to be inherited in an autosomal dominant fashion.
Paroxysmal kinesigenic dystonia after methylphenidate administration.
He described a disorder that was induced by sudden movements, and responded to anticonvulsants, naming it paroxysmal kinesigenic choreoathetosis.
Paroxysmal Kinesigenic Dyskinesia (PKD)
It is characterized by the association of benign familial infantile epilepsy (BIFE) at age 3-12 months and later in life with paroxysmal kinesigenic choreoathetosis.
There are three different subtypes of PD that include paroxysmal kinesigenic dyskinesia, paroxysmal non-kinesigenic dyskinesia, and paroxysmal exercise-induced dyskinesia.
Finally in a review in 1995 Demirkiran and Jankovic stated the disease should be called paroxysmal kinesigenic dyskinesia instead, pointing out that the attacks could manifest as any form of dyskinesia, not just choreoathetosis.
One variant known as infantile convulsions and choreoathetosis (ICCA) forms an association between BFIE and paroxysmal kinesigenic choreoathetosis and has been linked to the PRRT2 gene on chromosome 16.
Paroxysmal kinesigenic choreathetosis (PKC) also called Paroxysmal Kinesigenic Dyskinesia (PKD) is a hyperkinetic movement disorder characterized by attacks of involuntary movements, which are triggered by sudden voluntary movements.
