Diagnosis of Congenital Myasthenic Syndromes

J Gordon Millichap

doi:10.15844/pedneurbriefs-18-2-1

Diagnosis of Congenital Myasthenic Syndromes

Pediatric Neurology Briefs

Volume 18 (2004): Issue 2

By: J Gordon Millichap

Open Access

|Feb 2004

Abstract

Clinical and neurophysiological data of 11 patients (4 males, 7 females) with congenital myasthenic syndromes (CMS) diagnosed between 1994 and 2000 are reported from Great Ormond Street Hospital, London, UK.

References

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Millichap JG Dodge PR Diagnosis and treatment of myasthenia gravis in infancy, childhood, and adolescence: a study of 51 patients Neurology 1960 Nov 10 1007 1014 10.1212/WNL.10.7.643 13770917
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Engel AG Ohno K Congenital myasthenic syndromes Adv Neurol 2002 88 203 215 11908226
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Engel AG Nagel A Walls TJ Harper CM Waisburg HA Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptor Muscle Nerve 1993 Dec 16 12 1284 1292 10.1002/mus.880161204 8232383
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-18-2-1 | Journal eISSN: 2166-6482

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Language: English

Page range: 9 - 10

Published on: Feb 1, 2004

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Congenital Myasthenic Syndromes,

Myasthenia Gravis,

Profound Hypotonia

© 2004 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 18 (2004): Issue 2