Myoclonic Absence Seizures and Chromosome Anomalies

J Gordon Millichap

doi:10.15844/pedneurbriefs-12-7-9

Myoclonic Absence Seizures and Chromosome Anomalies

Pediatric Neurology Briefs

Volume 12 (1998): Issue 7

By: J Gordon Millichap

Open Access

|Jul 1998

Abstract

The relation between myoclonic absence-like seizures (MAS) and underlying chromosome disorders was evaluated in 14 patients at three centers in Italy.

References

Elia M Guerrini R Musumeci SA Bonanni P Gambardella A Aguglia U Myoclonic absence-like seizures and chromosome abnormality syndromes Epilepsia 1998 Jun 39 6 660 3 9637609 10.1111/j.1528-1157.1998.tb01435.x
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Mima T Nagamine T Ikeda A Yazawa S Kimura J Shibasaki H Pathogenesis of cortical myoclonus studied by magnetoencephalography Ann Neurol 1998 May 43 5 598 607 9585353 10.1002/ana.410430507
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-12-7-9 | Journal eISSN: 2166-6482

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Language: English

Page range: 53 - 54

Published on: Jul 1, 1998

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Chromosome Anomalies,

Shorter Absences,

Myoclonic Absence-Like Seizures

© 1998 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 12 (1998): Issue 7