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Publication Detail
Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Case Reports
  • Authors:
    Dale RC, Gardiner A, Antony J, Houlden H
  • Publication date:
    10/2012
  • Pagination:
    958, 960
  • Journal:
    Dev Med Child Neurol
  • Volume:
    54
  • Issue:
    10
  • Status:
    Published
  • Country:
    England
  • Language:
    eng
  • Keywords:
    Adult, Alleles, Child, Preschool, Chromosome Duplication, DNA Mutational Analysis, Dystonia, Epilepsy, Benign Neonatal, Female, Follow-Up Studies, Genotype, Humans, Infant, Male, Membrane Proteins, Migraine with Aura, Nerve Tissue Proteins, Pedigree, Phenotype, Pregnancy, Spasms, Infantile, Torticollis
Abstract
PRRT2 is the gene recently associated with paroxysmal kinesigenic dyskinesia (PKD), benign familial infantile epilepsy, and choreoathetosis infantile convulsions. We report four family members with PRRT2 mutations who had heterogeneous paroxysmal disorders. The index patient had transient infantile paroxysmal torticollis, then benign infantile epilepsy that responded to carbamazepine. The index patient's father had PKD and migraine with aphasia, and his two brothers had hemiplegic migraine with onset in childhood. All four family members had the same PRRT2 c.649dupC mutation. We conclude that heterogeneous paroxysmal disorders are associated with PRRT2 mutations and include paroxysmal torticollis and hemiplegic migraine. We propose that PRRT2 is a new gene for hemiplegic migraine.
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