Lambert-Eaton Syndrome in Children

J Gordon Millichap

doi:10.15844/pedneurbriefs-28-2-6

Lambert-Eaton Syndrome in Children

Pediatric Neurology Briefs

Volume 28 (2014): Issue 2

By: J Gordon Millichap

Open Access

|Feb 2014

Abstract

Investigators from Boston Children's Hospital; the Lahey Clinic, Burlington, MA; and Ohio State University, report 3 children presenting between ages 9 and 10 years with proximal lower extremity weakness with areflexia and low-amplitude compound muscle action potentials, and diagnosed with Lambert-Eaton myasthenic syndrome.

References

Hajjar M Markowitz J Darras BT Kissel JT Srinivasan J Jones HR Lambert-Eaton syndrome, an unrecognized treatable pediatric neuromuscular disorder: three patients and literature review Pediatr Neurol 2014 Jan 50 1 11 7 10.1016/j.pediatrneurol.2013.08.009 24138947
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Morgan-Followell B de Los Reyes E Child neurology: diagnosis of Lambert-Eaton myasthenic syndrome in children Neurology 2013 May 21 80 21 e220 2 10.1212/WNL.0b013e318293e14e 23690300
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-28-2-6 | Journal eISSN: 2166-6482

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Language: English

Page range: 12 - 13

Published on: Feb 1, 2014

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Proximal Lower Extremity,

Lymphoproliferative,

Immunomodulatory Therapy

© 2014 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 28 (2014): Issue 2