The Indian Journal of Pediatrics

, Volume 84, Issue 11, pp 877–878 | Cite as

KCNQ2 Epileptic Encephalopathy in Early Infancy

  • Ananthanarayanan Kasinathan
  • Naveen Sankhyan
  • Pratibha Singhi
Scientific Letter
  • 127 Downloads

References

  1. 1.
    Maljevic S, Lerche H. Potassium channel genes and benign familial neonatal epilepsy. Prog Brain Res. 2014;213:17–53.Google Scholar
  2. 2.
    Weckhuysen S, Mandelstam S, Suls A, et al. KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy. Ann Neurol. 2012;71:15–25.CrossRefPubMedGoogle Scholar
  3. 3.
    Kato M, Yamagata T, Kubota M, et al. Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation. Epilepsia. 2013;54:1282–7.CrossRefPubMedGoogle Scholar
  4. 4.
    Pisano T, Numis AL, Heavin SB, et al. Early and effective treatment of KCNQ2 encephalopathy. Epilepsia. 2015;56:685–91.CrossRefPubMedGoogle Scholar

Copyright information

© Dr. K C Chaudhuri Foundation 2017

Authors and Affiliations

  • Ananthanarayanan Kasinathan
    • 1
  • Naveen Sankhyan
    • 1
  • Pratibha Singhi
    • 1
  1. 1.Department of Pediatrics, Pediatric Neurology and Neurodevelopment Unit, Advanced Pediatrics CentrePostgraduate Institute of Medical Education and ResearchChandigarhIndia

Personalised recommendations