Infantile Epileptic Encephalopathies

J Gordon Millichap

doi:10.15844/pedneurbriefs-21-4-1

Infantile Epileptic Encephalopathies

Pediatric Neurology Briefs

Volume 21 (2007): Issue 4

By: J Gordon Millichap

Open Access

|Apr 2007

Abstract

The phenotypic variability associated with sodium channel alpha 1 subunit gene SCN1A mutations was studied in 188 patients with various infantile epileptic encephalopathies referred to the Universities of Adelaide and Melbourne, Australia; and centres in Glasgow, UK; Wellington, New Zealand; Montreal and Vancouver, Canada; Worcester, MD, USA, Israel, and Denmark.

References

Harkin LA McMahon JM Iona X Dibbens L Pelekanos JT Zuberi SM The spectrum of SCNIA-related infantile epileptic encephalopathies Brain 2007 March 130 Pt 3 843 852 10.1093/brain/awm002 17347258
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Jansen FE Sadleir LG Harkin LA Vadlamudi L McMahon JM Mulley JC Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults Neurology 2006 Dec 67 12 2224 6 10.1212/01.wnl.0000249312.73155.7d 17190949
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-21-4-1 | Journal eISSN: 2166-6482

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Language: English

Page range: 25 - 26

Published on: Apr 1, 2007

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

SMEI-Borderland,

Myoclonic-Astatic Epilepsy,

Dravet Syndrome

© 2007 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 21 (2007): Issue 4