Paroxysmal Kinesigenic Dyskinesia May Be Misdiagnosed in Co-occurring Gilles de la Tourette Syndrome.
作者信息
Ganos Christos, Mencacci Niccolo, Gardiner Alice, Erro Roberto, Batla Amit, Houlden Henry, Bhatia Kailash P
机构信息
Sobell Department of Motor Neuroscience and Movement Disorders UCL Institute of Neurology University College London London United Kingdom.
Department of Neurology University Medical Center Hamburg-Eppendorf (UKE) Hamburg Germany.
出版信息
Mov Disord Clin Pract. 2014 Apr 10;1(1):84-86. doi: 10.1002/mdc3.12001. eCollection 2014 Apr.
Abstract
摘要
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本文引用的文献
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Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations.发作性运动诱发性运动障碍患者伴或不伴 PRRT2 突变的临床遗传学比较。
Eur J Neurol. 2014 Apr;21(4):674-8. doi: 10.1111/ene.12142. Epub 2013 Mar 29.
2
Paroxysmal Kinesigenic Dyskinesia-like Symptoms in a Patient with Tourette Syndrome.一名抽动秽语综合征患者出现阵发性运动诱发性运动障碍样症状。
Tremor Other Hyperkinet Mov (N Y). 2011;1. doi: 10.7916/D8XG9PWK. Epub 2011 Dec 12.
3
Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations.儿童发作性运动诱发性运动障碍伴 PRRT2 基因突变的临床特征。
Dev Med Child Neurol. 2013 Apr;55(4):327-34. doi: 10.1111/dmcn.12056. Epub 2013 Jan 30.
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PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.家族性婴儿发作性癫痫、发作性运动障碍和偏瘫性偏头痛中的 PRRT2 突变。
Neurology. 2012 Nov 20;79(21):2109-14. doi: 10.1212/WNL.0b013e3182752ca2. Epub 2012 Oct 17.
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PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.PRRT2 基因突变：从发作性运动障碍到发作性共济失调和偏瘫性偏头痛。
Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17.
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Paroxysmal disorders associated with PRRT2 mutations shake up expectations on ion channel genes.与PRRT2突变相关的阵发性疾病颠覆了对离子通道基因的预期。
Neurology. 2012 Nov 20;79(21):2086-8. doi: 10.1212/WNL.0b013e3182752edd. Epub 2012 Oct 17.
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Neurology. 2012 Jul 10;79(2):170-4. doi: 10.1212/WNL.0b013e31825f06c3. Epub 2012 Jun 27.
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