Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lewis, R. A.
Right arrow Articles by Sumner, A. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lewis, R. A.
Right arrow Articles by Sumner, A. J.
NEUROLOGY 1982;32:592
© 1982 American Academy of Neurology

The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies

Richard A. Lewis, M.D. and Austin J. Sumner, M.D.

Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, PA.

We compared the electrodiagnostic studies of 40 patients with chronic acquired demyelinative neuropathy and 18 patients with familial demyelinative neuropathy. Patients with acquired neuropathy had differential slowing of conduction velocity when distal latencies were compared with more proximal conduction velocities in the same nerve, when equivalent segments of different nerves were compared, and when dispersion of compound motor action potentials was examined. Conduction block was noted in some patients. Patients with familial disease had uniform conduction slowing of all nerve segments, and conduction block was not seen.

Address correspondence and reprint requests to Dr. Lewis, Department of Neurology, University of Connecticut Health Center, and Farmington. CT 06032.

Chronic acquired demyelinative neuropathy is characterized by multifocal slowing of nerve conduction, whereas familial demyelinative neuropathy is characterized by uniform conduction slowing.

Presented in part at the thirty-second annual meeting of the American Academy of Neurology, New Orleans, LA, April 1980.

Accepted for publication October 28, 1981.




This article has been cited by other articles:


Home page
J. Neurol. Neurosurg. PsychiatryHome page
J Berciano, E Gallardo, A Garcia, J Infante, I Mateo, and O Combarros
Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study
J. Neurol. Neurosurg. Psychiatry, October 1, 2006; 77(10): 1169 - 1176.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
Z. A. Siddiqi, D. B. Sanders, and J. M. Massey
Peripheral neuropathy in Krabbe disease: electrodiagnostic findings.
Neurology, July 25, 2006; 67(2): 263 - 267.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
J. T. H. Van Asseldonk, L. H. Van den Berg, S. Kalmijn, J. H. J. Wokke, and H. Franssen
Criteria for demyelination based on the maximum slowing due to axonal degeneration, determined after warming in water at 37{degrees}C: diagnostic yield in chronic inflammatory demyelinating polyneuropathy
Brain, April 1, 2005; 128(4): 880 - 891.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
T. M. Burns
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Arch Neurol, June 1, 2004; 61(6): 973 - 975.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
L. Ginsberg, O. Malik, A. R. Kenton, D. Sharp, J. R. Muddle, M. B. Davis, J. B. Winer, R. W. Orrell, and R. H. M. King
Coexistent hereditary and inflammatory neuropathy
Brain, January 1, 2004; 127(1): 193 - 202.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
K. M. Krajewski, R. A. Lewis, D. R. Fuerst, C. Turansky, S. R. Hinderer, J. Garbern, J. Kamholz, and M. E. Shy
Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A
Brain, July 1, 2000; 123(7): 1516 - 1527.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
J Duarte, A C. Martinez, F Rodriguez, A Mendoza, A P Sempere, and L E Claveria
Hypertrophy of multiple cranial nerves and spinal roots in chronic inflammatory demyelinating neuropathy
J. Neurol. Neurosurg. Psychiatry, November 1, 1999; 67(5): 685 - 687.
[Full Text]


Home page
NEJMHome page
S. C. Gominak and D. P. Cros
Case 13-1998- A 23-Year-Old Man with Progressive Weakness and Paresthesias
N. Engl. J. Med., April 23, 1998; 338(17): 1212 - 1219.
[Full Text] [PDF]


Home page
NEJMHome page
S. C. Gominak and D. Cros
Case 41-1993- A 66-Year-Old Woman with a 19-Year History of Progressive Weakness of All Extremities
N. Engl. J. Med., October 14, 1993; 329(16): 1182 - 1190.
[Full Text]


Home page
Arch NeurolHome page
R. J. Barohn, J. T. Kissel, J. R. Warmolts, and J. R. Mendell
Chronic Inflammatory Demyelinating Polyradiculoneuropathy: Clinical Characteristics, Course, and Recommendations for Diagnostic Criteria
Arch Neurol, August 1, 1989; 46(8): 878 - 884.
[Abstract] [PDF]


Home page
Arch NeurolHome page
C. de Pablos, J. Calleja, O. Combarros, and J. Berciano
Spanish Toxic Oil Syndrome Neuropathy in Three Patients With Hereditary Motor and Sensory Neuropathy Type I
Arch Neurol, February 1, 1989; 46(2): 202 - 204.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1982 by AAN Enterprises, Inc.