HMSN I: Early Diagnosis

J Gordon Millichap

doi:10.15844/pedneurbriefs-6-11-10

HMSN I: Early Diagnosis

Pediatric Neurology Briefs

Volume 6 (1992): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1992

Abstract

The value of nerve conduction velocities in the detection of hereditary motor sensory neuropathy type I (HMSN I) in children at risk was determined in 36 children under 10 years of age at the University of Western Ontario, London, Ontario, Canada.

References

Feasby TE Hahn AF Bolton CF Brown WF Koopman WJ Hereditary motor sensory neuropathy type I in childhood J Neurol Neurosurg Psychiatry 1992 Oct 55 10 895 897 10.1136/jnnp.55.10.895 1331333
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Sghirlanzoni A Pareyson D Balestrini MR Bellone E Berta E Ciano C HMSN III phenotype due to homozygous expression of a dominant HMSN II gene Neurology 1992 Nov 42 11 2201 2204 10.1212/WNL.42.11.2201 1436537
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Jelloun-Dellagi SB Dellagi K Burger D Ben Younes-Chennoufi A Hentati FF Steck A Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0 Ann Neurol 1992 Nov 32 5 700 702 10.1002/ana.410320515 1280408
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-6-11-10 | Journal eISSN: 2166-6482

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Language: English

Page range: 86 - 87

Published on: Nov 1, 1992

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Hereditary Motor Sensory Neuropathy Type I,

Pes Planus,

Myelin Glycoprotein

© 1992 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 6 (1992): Issue 11