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Type: Artigo de periódico
Title: Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations
Author: Silveira-Moriyama, L
Gardiner, AR
Meyer, E
King, MD
Smith, M
Rakshi, K
Parker, A
Mallick, AA
Brown, R
Vassallo, G
Jardine, PE
Guerreiro, MM
Lees, AJ
Houlden, H
Kurian, MA
Abstract: Aim To define better the phenotype and genotype of familial and sporadic cases of paroxysmal kinesigenic dyskinesia (PKD) caused by mutations in the PRRT2 gene presenting in the paediatric age group. Method We report the detailed clinical and molecular genetic features of 11 patients (six females, five males) with childhood-onset PRRT2-mutation-positive PKD. Results Mean age at disease onset was 8years 7.5months (range 511y), and clinical presentation was characterized by daily short paroxysmal episodes of dystonia/dyskinesia. Most patients also had non-kinesigenic attacks in addition to the classical movement-induced paroxysmal episodes. One family demonstrated great phenotypic variability with PKD, infantile convulsions, and/or hemiplegic migraine affecting different family members with the same mutation. All patients in whom antiepileptics (carbamazepine/phenytoin) were tried showed a dramatic improvement with complete abolition of dyskinetic episodes. Interpretation Our case series provides a detailed clinical description of patients with PRRT2-PKD, and reports a spectrum of disease-causing mutations, thereby expanding both the clinical phenotype and mutation spectrum of disease.
Country: EUA
Editor: Wiley-blackwell
Citation: Developmental Medicine And Child Neurology. Wiley-blackwell, v. 55, n. 4, n. 327, n. 334, 2013.
Rights: fechado
Identifier DOI: 10.1111/dmcn.12056
Date Issue: 2013
Appears in Collections:Unicamp - Artigos e Outros Documentos

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