Literature DB >> 1513466

Autosomal recessive form of hereditary motor and sensory neuropathy type I.

A A Gabreëls-Festen1, F J Gabreëls, F G Jennekens, E M Joosten, T W Janssen-van Kempen.   

Abstract

We studied pathologic changes in sural nerve biopsies from four patients with probable autosomal recessive (AR) hereditary motor and sensory neuropathy (HMSN) type I with a median motor nerve conduction velocity greater than 10 m/sec, comparing them with the pathologic features in autosomal dominant (AD) HMSN type I. The four recessive and two sporadic cases showed segmental demyelination. However, the classic onion bulbs of concentric Schwann cell processes, which occur in AD type I, were rare; many axons, also of a smaller size, were surrounded by onion bulbs of basal laminae. Schwann cells of the myelinated and unmyelinated types were involved in these onion bulb formations. Patients with HMSN type I who have many basal lamina onion bulbs should be considered as having AR inheritance.

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Year:  1992        PMID: 1513466     DOI: 10.1212/wnl.42.9.1755

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


  9 in total

1.  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 2.  Animal models for inherited peripheral neuropathies.

Authors:  R Martini
Journal:  J Anat       Date:  1997-10       Impact factor: 2.610

3.  Homozygous hypertrophic hereditary motor and sensory neuropathies.

Authors:  A Sghirlanzoni; D Pareyson; R Marazzi; G Cavaletti; E Bellone; P Mandich; M R Balestrini; D Riva
Journal:  Ital J Neurol Sci       Date:  1994-02

4.  Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.

Authors:  A A Gabreëls-Festen; F J Gabreëls; J E Hoogendijk; P A Bolhuis; P J Jongen; H M Vingerhoets
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

5.  SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system.

Authors:  Estelle Arnaud; Jennifer Zenker; Anne-Sophie de Preux Charles; Claudia Stendel; Andreas Roos; Jean-Jacques Médard; Nicolas Tricaud; Henning Kleine; Bernhard Luscher; Joachim Weis; Ueli Suter; Jan Senderek; Roman Chrast
Journal:  Proc Natl Acad Sci U S A       Date:  2009-09-29       Impact factor: 11.205

6.  Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutations.

Authors:  A A Gabreëls-Festen; P A Bolhuis; J E Hoogendijk; L J Valentijn; E J Eshuis; F J Gabreëls
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

7.  Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patients.

Authors:  F Schiavon; M L Mostacciuolo; F Saad; L Merlini; G Siciliano; C Angelini; G A Danieli
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

8.  Rapid Identification of Pathogenic Variants in Two Cases of Charcot-Marie-Tooth Disease by Gene-Panel Sequencing.

Authors:  Chi-Chun Ho; Shuk-Mui Tai; Edmond Chi-Nam Lee; Timothy Shin-Heng Mak; Timothy Kam-Tim Liu; Victor Wai-Lun Tang; Wing-Tat Poon
Journal:  Int J Mol Sci       Date:  2017-04-05       Impact factor: 5.923

9.  Neuronal activity in the hub of extrasynaptic Schwann cell-axon interactions.

Authors:  Chrysanthi Samara; Olivier Poirot; Enric Domènech-Estévez; Roman Chrast
Journal:  Front Cell Neurosci       Date:  2013-11-25       Impact factor: 5.505

  9 in total

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