Genetics of headache in children: where are we headed?

Curr Pain Headache Rep. 2008 Oct;12(5):367-72. doi: 10.1007/s11916-008-0062-x.

Abstract

A history of headaches in a family is very frequently noted when evaluating a child for recurrent, episodic headaches. Oftentimes, these headaches have migraine features, although the family may deny a history of migraine. This positive family history implies an inherited or genetic basis as a component to the underlying pathophysiology of primary headaches. A variety of methodology has begun to elucidate this contribution, including historical observation, population-based studies of families and twins, gene polymorphism association studies, and specific gene identification for isolated migraine subtypes. This line of investigation should progress in the future to a better understanding of migraine and clarification of the diagnostic subtypes for a genotype-phenotype association.

Publication types

  • Review

MeSH terms

  • Child
  • Chromosomes, Human, Pair 1 / genetics
  • Headache / diagnosis
  • Headache / genetics*
  • Humans
  • NAV1.1 Voltage-Gated Sodium Channel
  • Nerve Tissue Proteins / genetics
  • Severity of Illness Index
  • Small-Conductance Calcium-Activated Potassium Channels / genetics
  • Sodium Channels / genetics
  • Sodium-Potassium-Exchanging ATPase / genetics
  • Twin Studies as Topic

Substances

  • KCNN3 protein, human
  • NAV1.1 Voltage-Gated Sodium Channel
  • Nerve Tissue Proteins
  • SCN1A protein, human
  • Small-Conductance Calcium-Activated Potassium Channels
  • Sodium Channels
  • ATP1A2 protein, human
  • Sodium-Potassium-Exchanging ATPase