Literature DB >> 2779605

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding.

A Ohnishi1, Y Murai, M Ikeda, T Fujita, H Furuya, Y Kuroiwa.   

Abstract

Two Japanese persons with consanguinous parents had a motor and sensory neuropathy of the hypertrophic type with excessive myelin outfolding in the myelinated fibers. A morphometric analysis of the biopsied sural nerve was made. Excessive myelin outfolding, segmental demyelination, and remyelination and decrease in the density of both large and small myelinated fibers were evident. Using linear regression, myelin spiral length was shorter relative to axonal area. These patients may have a new variant of hereditary motor sensory neuropathy.

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Year:  1989        PMID: 2779605     DOI: 10.1002/mus.880120707

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  21 in total

1.  Fine structural evaluation of altered Schmidt-Lanterman incisures in human sural nerve biopsies.

Authors:  J M Schröder; F Himmelmann
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

2.  An unusual demyelinating neuropathy in a patient with Waardenburg's syndrome.

Authors:  J M Jacobs; J Wilson
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

3.  Infantile neuropathy with unstable myelin: study of the P0 protein.

Authors:  S Peudenier; J F Deleuze; D Pham-Dinh; C Lacroix; J Boulloche; P Landrieu
Journal:  J Neurol       Date:  1993-05       Impact factor: 4.849

4.  Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.

Authors:  A Gabreëls-Festen; S van Beersum; L Eshuis; E LeGuern; F Gabreëls; B van Engelen; E Mariman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-05       Impact factor: 10.154

Review 5.  Neuropathology of Charcot-Marie-Tooth and related disorders.

Authors:  J Michael Schröder
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

6.  Smaller number of large myelinated fibers and focal myelin thickening in mutant quails deficient in neurofilaments.

Authors:  J X Zhao; A Ohnishi; C Itakura; M Mizutani; T Yamamoto; H Hayashi; Y Murai
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

7.  Greater number of microtubules per axon of unmyelinated fibers of mutant quails deficient in neurofilaments: possible compensation for the absence of neurofilaments.

Authors:  J X Zhao; A Ohnishi; C Itakura; M Mizutani; T Yamamoto; H Hayashi; Y Murai
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

Review 8.  [Genetics of neuropathies].

Authors:  B Gess; A Schirmacher; P Young
Journal:  Nervenarzt       Date:  2013-02       Impact factor: 1.214

9.  Loss of the inactive myotubularin-related phosphatase Mtmr13 leads to a Charcot-Marie-Tooth 4B2-like peripheral neuropathy in mice.

Authors:  Fred L Robinson; Ingrid R Niesman; Kristina K Beiswenger; Jack E Dixon
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-18       Impact factor: 11.205

Review 10.  Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Authors:  Anneke Gabreëls-Festen
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

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