Phenotypes, genotypes, and the management of paroxysmal movement disorders.

Laura Silveira-MoriyamaStjepana KovacManju A KurianHenry HouldenAndrew J LeesMatthew C WalkerEmmanuel RozeAlex R PaciorkowskiJonathan W MinkThomas T Warner

Published in: Developmental medicine and child neurology (2018)

A growing number of genes have been associated with classic and newly described paroxysmal movement disorders. Paroxysmal movement disorders share common mechanisms and clinical features with other neurological paroxysmal phenomena including epilepsy and migraine.

Keyphrases

atrial fibrillation
catheter ablation
gene expression
brain injury
genome wide analysis