Literature DB >> 3002086

Congenital neuropathy with prevailing axonal changes. A clinical and histological report.

F Guzzetta, G Ferrière.   

Abstract

A case of congenital neuropathy associated with an unclassified chronic brain disorder is described. Morphological findings differ from the reported congenital neuropathies where primary myelin change have been usually found. In contrast, sural nerve biopsy showed marked signs of active or past axonal degeneration; at the teasing and morphometric analysis there was also some evidence of segmental demyelination. Atypical onion bulb formations (Evans and Murray type) and a very poor demyelination activity stressed the prevailing axonal involvement with possibly secondary segmental demyelination.

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Year:  1985        PMID: 3002086     DOI: 10.1007/bf00690192

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  23 in total

1.  A case of congenital hypomyelination neuropathy. Clinical, morphological, and chemical studies.

Authors:  W R Kennedy; J H Sung; J F Berry
Journal:  Arch Neurol       Date:  1977-06

Review 2.  Polyneuropathy in childhood.

Authors:  I Gamstorp
Journal:  Acta Paediatr Scand       Date:  1968-05

3.  The normal sural nerve in man. II. Changes in the axons and Schwann cells due to ageing.

Authors:  J Ochoa; W G Mair
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

4.  Changes of the ratio between myelin thickness and axon diameter in the human developing sural nerve.

Authors:  J M Schröder; J Bohl; K Brodda
Journal:  Acta Neuropathol       Date:  1978-08-07       Impact factor: 17.088

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Authors:  C Palix; J Coignet
Journal:  Pediatrie       Date:  1978-03

6.  Polyneuropathy in childhood.

Authors:  O B Evans
Journal:  Pediatrics       Date:  1979-07       Impact factor: 7.124

7.  Connatal polyneuropathy -- a case with proliferated microfilaments in Schwann cells.

Authors:  J Ulrich; H R Hirt; P Kleihues; M Oberholzer
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

8.  The nosology of genetic peripheral neuropathies in Swedish children.

Authors:  B Hagberg; B Westerberg
Journal:  Dev Med Child Neurol       Date:  1983-02       Impact factor: 5.449

9.  Congenital hypomyelination neuropathy in a newborn.

Authors:  S Hakamada; T Kumagai; K Hara; S Miyazaki; K Miyazaki; K Watanabe
Journal:  Neuropediatrics       Date:  1983-08       Impact factor: 1.947

10.  Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood.

Authors:  M Vanasse; V Dubowitz
Journal:  Muscle Nerve       Date:  1981 Jan-Feb       Impact factor: 3.217

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  3 in total

1.  Variability of morphological features in early infantile polyneuropathy with defective myelination.

Authors:  A Vital; C Vital; J P Riviere; C Brechenmacher; J Marot
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

2.  Congenital hypomyelination with axonopathy.

Authors:  A Vital; C Vital; M Coquet; X Hernandorena; J M Demarquez
Journal:  Eur J Pediatr       Date:  1989-02       Impact factor: 3.183

Review 3.  Polyneuropathies in paediatrics.

Authors:  B Hagberg
Journal:  Eur J Pediatr       Date:  1990-02       Impact factor: 3.183

  3 in total

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