Autosomal Dominant Epilepsy Syndrome Linked to 2p11

J Gordon Millichap

doi:10.15844/pedneurbriefs-16-1-4

Autosomal Dominant Epilepsy Syndrome Linked to 2p11

Pediatric Neurology Briefs

Volume 16 (2002): Issue 1

By: J Gordon Millichap

Open Access

|Jan 2002

Abstract

A newly recognized autosomal dominant epilepsy syndrome with linkage to chromosome 2p11.1-q12.2 is described in an Italian pedigree of 8 patients reported from the Neurosciences Unit, Institute of Child Health and Great Ormond Street Hospital for Children, London, UK.

References

Guerrini R Bonanni P Patrignani A Brown P Parmeggiani L Grosse P Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2 Brain 2001 Dec 124 Pt 12 2459 75 10.1093/brain/124.12.2459 11701600
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-16-1-4 | Journal eISSN: 2166-6482

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Language: English

Page range: 3 - 4

Published on: Jan 1, 2002

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Valproate,

Contralateral Rolandic Area,

Cortical Origin

© 2002 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 16 (2002): Issue 1