Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsy
Author:
Affiliation:
1. Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India,
Publisher
Scientific Scholar
Subject
Neurology (clinical),General Neuroscience
Reference5 articles.
1. PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine;Gardiner;Neurology,2012
2. PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions;Van Vliet;Neurology,2012
3. Diagnosis and treatment of paroxysmal dyskinesias revisited;Unterberger;Ther Adv Neurol Disord,2008
4. Characteristics of infantile convulsions and choreoathetosis syndrome caused by PRRT2 mutation;Deng;Pediatr Investig,2022
5. Case report: Long-term suppression of paroxysmal kinesigenic dyskinesia after bilateral thalamotomy;Murakami;Front Neurol,2021
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