Epilepsy with Myoclonic Absences

J Gordon Millichap

doi:10.15844/pedneurbriefs-8-6-4

Epilepsy with Myoclonic Absences

Pediatric Neurology Briefs

Volume 8 (1994): Issue 6

By: J Gordon Millichap

Open Access

|Jun 1994

Abstract

Resistance to therapy and learning disabilities are stressed as frequent complications of the syndrome of “epilepsy with myoclonic absences” reported in 8 children, ages 6 to 16 years, seen at the University Hospital of Wales in a 10 year period.

References

Manonmani V Wallace SJ Epilepsy with myoclonic absences Arch Dis Child 1994 Apr 70 4 288 90 8185360 10.1136/adc.70.4.288
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Schlumberger E Chavez F Palacios L Rey E Pajot N Dulac O Lamotrigine in treatment of 120 children with epilepsy Epilepsia 1994 Mar-Apr 35 2 359 67 8156958 10.1111/j.1528-1157.1994.tb02445.x
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-8-6-4 | Journal eISSN: 2166-6482

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Language: English

Page range: 43 - 43

Published on: Jun 1, 1994

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Myoclonic Absences,

Upper Limbs,

Cerebellar Ataxia

© 1994 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 8 (1994): Issue 6