Paroxysmal kinesigenic dyskinesia (PKD): clinical features
Evidence-based neurology checklist on paroxysmal kinesigenic dyskinesia (pkd): clinical features: Genetic mutations PRRT2 gene TMEM151A gene PRRT2 gene mutation related disorders Triggers for attacks Aura symptoms Dyskinesia features Associated movement disorders Associated epileptic disorders…
Genetic mutations
- PRRT2 gene
- TMEM151A gene
PRRT2 gene mutation related disorders
Triggers for attacks
Aura symptoms
Dyskinesia features
Associated movement disorders
Associated epileptic disorders
Other associated neurological disorders
Distinctive features of PRRT2 PKD
Outcome and prognosis
Synonyms
References
- Muller U. The monogenic primary dystonias. Brain 2009; 132:2005-2025.
- Albanese A, Asmus F, Bhatia KP, et al. EFNS guidelines on diagnosis and treatment of primary dystonias. Eur J Neurol 2011; 18:5-18.
- Ledoux MS, Dauer WT, Warner TT. Emerging common molecular pathways for primary dystonia. Mov Disord 2013; 28:968-981.
- Fabbri M, Marini C, Bisulli F, et al. Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation. Epileptic Disord 2013; 15:123-127.
- Bruno MK, Hallett M, Gwinn-Hardy K, et al. Clinical evaluation of idiopathic kinesigenic dyskinesia: new diagnostic criteria. Neurology 2004; 63:2280-2287.
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