Idiopathic paroxysmal kinesigenic dyskinesia in Malaysia, a multi-racial Southeast Asian country

Tai, Mei-Ling.S. and Lim, Shen-Yang and Tan, C.T. (2010) Idiopathic paroxysmal kinesigenic dyskinesia in Malaysia, a multi-racial Southeast Asian country. Journal of Clinical Neuroscience, 17 (8). pp. 1089-1090.

Full text not available from this repository.

Abstract

Paroxysmal kinesigenic dyskinesia is a rare disorder, and there are few reports of Asian patients with this condition. We reviewed the clinical features of all patients with idiopathic paroxysmal kinesigenic dyskinesia (PKD) seen at a major neurological centre in Malaysia. The charts of 11 patients with idiopathic PKD seen between 1995 and 2008 were reviewed retrospectively. The male:female ratio was 9:2. Ten patients were of Chinese ethnicity, and one was Malay. Three patients (from two families) had a family history of PKD. The involuntary movement was dystonia in 73% of patients. In one patient, attacks were precipitated by vestibular stimulation. One patient had generalized epilepsy. Another patient who did not have epilepsy demonstrated epileptiform discharges. Only slightly over one-quarter of patients had a positive family history. Males, and people of Chinese ancestry, seem to be affected more frequently by MD in certain Asian populations. (C) 2010 Elsevier Ltd. All rights reserved.

Item Type: Article
Funders: UNSPECIFIED
Uncontrolled Keywords: Paroxysmal kinesigenic dyskinesia (PKD); Idiopathic; Southeast Asian
Subjects: R Medicine
Depositing User: Mr Faizal 2
Date Deposited: 09 Feb 2015 04:49
Last Modified: 09 Feb 2015 04:49
URI: http://eprints.um.edu.my/id/eprint/12642

Actions (login required)

View Item View Item