Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier

Massimo Marano, Francesco Motolese, Federica Consoli, Alessandro De Luca, Vincenzo Di Lazzaro

Research output: Contribution to journalReview articlepeer-review

Abstract

Background: Paroxysmal movement disorders are rare and heterogeneous genetic conditions characterized by the recurrence of transient involuntary movements. Phenomenology Shown: The phenomenology of a paroxysmal kinesigenic dyskinesia in a young professional athlete. Educational Value: Providing basic clinical and genetic elements for the early recognition and diagnosis of a rare movement disorder.

Original languageEnglish
Number of pages1
JournalTremor and other hyperkinetic movements (New York, N.Y.)
Volume8
DOIs
Publication statusPublished - Jan 1 2018

Keywords

  • dystonia
  • Paroxysmal dyskinesia
  • paroxysmal exercise‐induced dyskinesia
  • paroxysmal kinesigenic dyskinesia
  • paroxysmal non‐kinesigenic dyskinesia
  • PRRT2

Fingerprint

Dive into the research topics of 'Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier'. Together they form a unique fingerprint.

Cite this