Hereditary Motor and Sensory Neuropathy IIB

J Gordon Millichap

doi:10.15844/pedneurbriefs-11-2-8

Hereditary Motor and Sensory Neuropathy IIB

Pediatric Neurology Briefs

Volume 11 (1997): Issue 2

By: J Gordon Millichap

Open Access

|Feb 1997

Abstract

The clinical and electrodiagnostic features of 10 adults in a family with axonal, autosomal dominant, hereditary motor and sensory neuropathy (HMSN IIB), with linkage to chromosome 3q, are reported from Washington University School of Medicine, St Louis, MO.

References

Elliott JL Kwon JM Goodfellow PJ Yee W-C Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics Neurology 1997 Jan 48 1 23 28 10.1212/WNL.48.1.23 9008488
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Marrosu MG Vaccargiu S Marrosu G Vannelli A Cianchetti C Muntoni F A novel point mutation in the peripheral myelin protein 22 (PMP22) gene associated with Charcot-Marie-Tooth disease type 1A Neurology 1997 Feb 48 2 489 493 10.1212/WNL.48.2.489 9040744
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-11-2-8 | Journal eISSN: 2166-6482

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Language: English

Page range: 13 - 14

Published on: Feb 1, 1997

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Hereditary Motor and Sensory Neuropathy,

Hypertrophic Nerves,

Homogeneous Entity

© 1997 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 11 (1997): Issue 2