Article
Phenotypes, genotypes, and the management of paroxysmal movement disorders.
Developmental medicine and child neurology - 1 Jun 2018
Silveira-Moriyama Laura, Kovac Stjepana, Kurian Manju A, Houlden Henry, Lees Andrew J, Walker Matthew C, Roze Emmanuel, Paciorkowski Alex R, Mink Jonathan W, Warner Thomas T
Abstract excerpt
As a consequence of the genomic revolution, a large number of publications describing paroxysmal movement disorders have been published in the last few years, shedding light on their molecular pathology. Routine gene testing is not necessary to guide treatment for typical forms of paroxysmal kinesigenic dyskinesia (PKD), paroxysmal nonkinesigenic dyskinesia (PNKD), and episodic ataxia type 1 or 2. It can,...
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