TY - JOUR
T1 - Paroxysmal Dyskinesias in a PRRT2 Mutation Carrier
AU - Marano, Massimo
AU - Motolese, Francesco
AU - Consoli, Federica
AU - De Luca, Alessandro
AU - Di Lazzaro, Vincenzo
PY - 2018/1/1
Y1 - 2018/1/1
N2 - 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.
AB - 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.
KW - dystonia
KW - Paroxysmal dyskinesia
KW - paroxysmal exercise‐induced dyskinesia
KW - paroxysmal kinesigenic dyskinesia
KW - paroxysmal non‐kinesigenic dyskinesia
KW - PRRT2
UR - http://www.scopus.com/inward/record.url?scp=85059796605&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85059796605&partnerID=8YFLogxK
U2 - 10.7916/D8S488X0
DO - 10.7916/D8S488X0
M3 - Review article
C2 - 30622840
AN - SCOPUS:85059796605
VL - 8
JO - Tremor and other hyperkinetic movements (New York, N.Y.)
JF - Tremor and other hyperkinetic movements (New York, N.Y.)
SN - 2160-8288
ER -