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Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
oleh: Massimo Marano, Francesco Motolese, Federica Consoli, Alessandro De Luca, Vincenzo Di Lazzaro
Format: | Article |
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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.