A Case of KCNQ2-Associated Movement Disorder Triggered by Fever

J Child Neurol. 2017 Dec;32(14):1123-1124. doi: 10.1177/0883073817736702.

Abstract

The differential diagnosis of fever-induced movement disorders in childhood is broad. Whole exome sequencing has yielded new insights into those cases with a suspected genetic basis. We report the case of an 8-year-old boy with a history of neonatal seizures who presented with near-continuous hyperkinetic movements of his limbs during a febrile illness. Initial diagnostic testing did not explain his abnormalities; however, given the suspicion for a channelopathy, whole exome sequencing was performed and it demonstrated a de novo pathogenic heterozygous variant in KCNQ2. There is an expanding phenotypic spectrum of heterozygous alterations in KCNQ2; however, this report provides the first description of a pathogenic KCNQ2 variant fever-induced hyperkinetic movement disorder in childhood. We also review the literature of cases previously published with the same pathogenic variant.

Keywords: chorea; genetics; mutation; next generation sequencing; pediatrics.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Electroencephalography
  • Family Health*
  • Fever / complications*
  • Humans
  • KCNQ2 Potassium Channel / genetics*
  • Male
  • Movement Disorders / etiology*
  • Movement Disorders / genetics*
  • Mutation / genetics*

Substances

  • KCNQ2 Potassium Channel
  • KCNQ2 protein, human