A case of congenital myopathy masquerading as paroxysmal dyskinesia

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Paroxysmal Kinesigenic Dyskinesia

Background Paroxysmal kinesigenic dyskinesia (PKD) is a rare condition associated with heterozygous mutations in the proline-rich transmembrane protein 2 (PRRT2) gene. Phenomenology Shown In this article we illustrate the phenomenology of PKD in a male previously misdiagnosed with Tourette's syndrome. Educational Value Regardless of the underlying phenotype, PKD is highly responsive to some...

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We present a case of paroxysmal kinesigenic dyskinesia (PKD) in a 21 year old girl, with no family history of similar episodes. The episodes were short (lasting less than a minute), frequent, occurring 5 to 10 times a day, self-limiting dystonia of her right upper limb precipitated by sudden movement. She also had a past history of partial seizures with secondary generalization in her childhood...

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ژورنال

عنوان ژورنال: Annals of Indian Academy of Neurology

سال: 2014

ISSN: 0972-2327

DOI: 10.4103/0972-2327.144034