Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier

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

Format: Article
Diterbitkan: Ubiquity Press 2018-12-01

Deskripsi

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.