Literature DB >> 6865475

Minimal pathologic expression of a mutant gene for hereditary motor and sensory neuropathy.

P J Dyck, J L Karnes, A J Windebank, M Sparks, J C Stevens, P C O'Brien.   

Abstract

Transverse sections of the sural nerve of a 46-year-old woman without neuropathic symptoms or abnormalities on nerve conduction, electromyography, or computer-assisted sensory examination contained minute regions with large onion bulbs intermingled with normal-appearing myelinated fibers and surrounded by fields of normal myelinated fibers. This woman's 19-year-old daughter had long-standing hypertrophic neuropathy with diffusely distributed large onion bulbs. Computer-imaging reconstruction of myelinated fibers and teased myelinated fiber studies of fascicles containing focal regions with onion bulbs of the mother's nerve provided evidence that onion bulbs surrounded atrophic axons with short internodes and demyelination. This is the least expression for inherited neuropathy which has been reported. These findings therefore suggest that an inherited neuropathy may be minimally expressed by a pathologic alteration of only selected neurons (axons).

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Year:  1983        PMID: 6865475

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  1 in total

1.  Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2.

Authors:  B H Holmberg; G Holmgren; E Nelis; C van Broeckhoven; B Westerberg
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

  1 in total

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