Literature DB >> 12084875

Hereditary neuropathy with liability to pressure palsy: the electrophysiology fits the name.

Jun Li1, Karen Krajewski, Michael E Shy, Richard A Lewis.   

Abstract

BACKGROUND: Studies of patients with hereditary neuropathy with liability to pressure palsies (HNPP) have shown accentuated distal slowing along with nonuniform conduction abnormalities at segments liable to compression, suggesting a distal myelinopathy as an underlying pathophysiological mechanism.
METHODS: We evaluated 12 patients with HNPP by standard nerve conduction studies and by conduction to more proximal muscles in the arm and leg. Three CMT1A patients and six healthy subjects also were evaluated as controls.
RESULTS: Median and peroneal motor nerves in all HNPP patients showed prolonged distal motor latencies (DML) (mean +/- SE, 5.9 +/- 0.41 and 8.63 +/- 0.58 milliseconds), but the ulnar and tibial DML were minimally prolonged or normal (mean +/- SE, 3.87 +/- 0.16 and 5.66 +/- 0.24 milliseconds). DML to forearm flexor (median and ulnar nerves) or anterior tibial muscles (peroneal nerve) were also normal.
CONCLUSION: Accentuated distal slowing is found primarily in median and peroneal nerve segments liable to pressure palsies or repetitive trauma. However, the ulnar and tibial nerves, which are less liable to compression, have minimal changes. In addition, distal latencies to more proximal muscles in the arm and leg do not have distal slowing. These findings do not support a distal myelinopathy as a determinant of the conduction abnormalities in HNPP.

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Mesh:

Year:  2002        PMID: 12084875     DOI: 10.1212/wnl.58.12.1769

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  35 in total

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2.  Charcot-Marie-Tooth disease subtypes and genetic testing strategies.

Authors:  Anita S D Saporta; Stephanie L Sottile; Lindsey J Miller; Shawna M E Feely; Carly E Siskind; Michael E Shy
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Review 3.  Inherited neuropathies.

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Journal:  Semin Neurol       Date:  2012-11-01       Impact factor: 3.420

Review 4.  A review of genetic counseling for Charcot Marie Tooth disease (CMT).

Authors:  Carly E Siskind; Seema Panchal; Corrine O Smith; Shawna M E Feely; Joline C Dalton; Alice B Schindler; Karen M Krajewski
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5.  Neuropathy in a human without the PMP22 gene.

Authors:  Mario Andre Saporta; Istvan Katona; Xuebao Zhang; Helen P Roper; Louise McClelland; Fiona Macdonald; Louise Brueton; Julian Blake; Ueli Suter; Mary M Reilly; Michael E Shy; Jun Li
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6.  Proximal nerve magnetization transfer MRI relates to disability in Charcot-Marie-Tooth diseases.

Authors:  Richard D Dortch; Lindsey M Dethrage; John C Gore; Seth A Smith; Jun Li
Journal:  Neurology       Date:  2014-09-24       Impact factor: 9.910

Review 7.  The PMP22 gene and its related diseases.

Authors:  Jun Li; Brett Parker; Colin Martyn; Chandramohan Natarajan; Jiasong Guo
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Review 8.  Diagnosis of Charcot-Marie-Tooth disease.

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9.  Classification and diagnosis of the inherited neuropathies.

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Journal:  Ann Indian Acad Neurol       Date:  2009-04       Impact factor: 1.383

10.  Conduction block in PMP22 deficiency.

Authors:  Yunhong Bai; Xuebao Zhang; Istvan Katona; Mario Andre Saporta; Michael E Shy; Heather A O'Malley; Lori L Isom; Ueli Suter; Jun Li
Journal:  J Neurosci       Date:  2010-01-13       Impact factor: 6.167

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