Literature DB >> 20387208

[Familial idiopathic paroxysmal kinesigenic dyskinesia: its natural history and a descriptive study in three Spanish families].

Juan Palau-Bargues1, Ignacio Rubio-Agusti, Juan Andrés Burguera, Juan Jesús Vilchez-Padilla, Vicente E Villanueva.   

Abstract

INTRODUCTION: Paroxysmal kinesigenic dyskinesia (PKD) is a disorder that is characterised by brief episodes of involuntary movements triggered by other sudden movements. PATIENTS AND METHODS: Here we describe the cases of nine patients from three unrelated families who had PKD in its familial idiopathic form.
RESULTS: The majority of the patients (77.7%) were males. The mean age at onset was 10.3 years. All the subjects presented sudden movements as factors that precipitated the crises, which lasted < 10 s in 88.8% of cases. Two thirds (66.6%) of the patients were treated with carbamazepine, phenytoin and valproic acid and all of them responded well. Spontaneous remission occurred in 62.5% of the patients over 20 years of age and in a further 25% there was a significant decrease in the number of crises.
CONCLUSIONS: In our sample the proportion of patients who presented spontaneous remission was greater than in that reported in previous studies. As in other series, we found positive responses to antiepileptic drugs other than carbamazepine.

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Year:  2010        PMID: 20387208

Source DB:  PubMed          Journal:  Rev Neurol        ISSN: 0210-0010            Impact factor:   0.870


  1 in total

1.  Case Report: Long-Term Suppression of Paroxysmal Kinesigenic Dyskinesia After Bilateral Thalamotomy.

Authors:  Masato Murakami; Shiro Horisawa; Kenko Azuma; Hiroyuki Akagawa; Taku Nonaka; Takakazu Kawamata; Takaomi Taira
Journal:  Front Neurol       Date:  2021-12-03       Impact factor: 4.003

  1 in total

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