Early-Onset Epileptic Encephalopathies with STXBPl Mutations

J Gordon Millichap

doi:10.15844/pedneurbriefs-24-12-1

Early-Onset Epileptic Encephalopathies with STXBPl Mutations

Pediatric Neurology Briefs

Volume 24 (2010): Issue 12

By: J Gordon Millichap

Open Access

|Dec 2010

Abstract

Researchers at the Department of Molecular Genetics, University of Antwerp, and other centers in Belgium, The Netherlands, and Melbourne, Australia, analyzed the clinical phenotypes associated with STXBPl mutations in a cohort of 106 patients with unexplained early-onset epileptic encephalopathies.

References

Deprez L Weckhuysen S Holmgren P Suls A Van Dyck T Goossens D Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations Neurology 2010 Sep 28 75 13 1159 65 10.1212/WNL.0b013e3181f4d7bf 20876469
Open DOI Search in Google Scholar Back to article
Holland KD Hallinan BE What causes epileptic encephalopathy in infancy?: the answer may lie in our genes Neurology 2010 Sep 28 75 13 1132 3 10.1212/WNL.0b013e3181f6bc97 20876466
Open DOI Search in Google Scholar Back to article
Millichap JJ Koh S Laux LC Nordli DR Jr Child Neurology: Dravet syndrome: when to suspect the diagnosis Neurology 2009 Sep 29 73 13 e59 62 10.1212/WNL.0b013e3181b9c880 19786689
Open DOI Search in Google Scholar Back to article

Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-24-12-1 | Journal eISSN: 2166-6482

Journal RSS Feed

Language: English

Page range: 89 - 90

Published on: Dec 1, 2010

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Early Myoclonic Encephalopathy,

Early-Onset Epileptic Encephalopathy,

Ohtahara Syndrome

© 2010 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 24 (2010): Issue 12