Literature DB >> 3673511

Congenital hypo- and hypermyelination neuropathy. Two cases.

J M Vallat1, R Gil, M J Leboutet, J Hugon, D Moulies.   

Abstract

Two young patients were referred recently to the authors for investigation of a peroneal atrophy syndrome. Since the first symptoms were observed in infancy, a congenital hypomyelination neuropathy was suspected, and superficial peroneal nerve biopsies were taken. Signs of severe and widespread demyelination/remyelination were observed. These features appeared morphologically similar to those observed in the globular or tomaculous neuropathies. The mechanism of the hypermyelination is discussed.

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Year:  1987        PMID: 3673511     DOI: 10.1007/bf00692853

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


  18 in total

1.  Infantile polyneuropathy with defective myelination: an autopsy study.

Authors:  S B Karch; H Urich
Journal:  Dev Med Child Neurol       Date:  1975-08       Impact factor: 5.449

2.  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

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Authors:  F Behse; F Buchthal; F Carlsen; G G Knappeis
Journal:  Brain       Date:  1972       Impact factor: 13.501

4.  Globular neuropathy. A disorder of axons and Schwann cells.

Authors:  A D Dayan; G S Graveson; P K Robinson; M A Woodhouse
Journal:  J Neurol Neurosurg Psychiatry       Date:  1968-12       Impact factor: 10.154

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Journal:  Scott Med J       Date:  1970-03       Impact factor: 0.729

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

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.  Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life.

Authors:  F Guzzetta; G Ferrière; G Lyon
Journal:  Brain       Date:  1982-06       Impact factor: 13.501

9.  Congenital hypomyelinating neuropathy.

Authors:  Y Harati; I J Butler
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-12       Impact factor: 10.154

10.  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

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  11 in total

1.  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

2.  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

Review 3.  Neuropathology of Charcot-Marie-Tooth and related disorders.

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

4.  Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies.

Authors:  S Sander; R A Ouvrier; J G McLeod; G A Nicholson; J D Pollard
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-04       Impact factor: 10.154

5.  An autopsy case of peroneal muscular atrophy with rigidity and tremor. Ultrastructural and systematic morphometrical studies on peripheral nerves.

Authors:  Y Itoh; S Yagishita; N Amano; K Iwabuchi
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

6.  Autosomal recessive forms of Charcot-Marie-Tooth disease.

Authors:  J M Vallat; D Grid; C Magdelaine; F Sturtz; M Tazir
Journal:  Curr Neurol Neurosci Rep       Date:  2004-09       Impact factor: 5.081

Review 7.  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

8.  Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex.

Authors:  F Umehara; S Takenaga; M Nakagawa; K Takahashi; S Izumo; K Matsumuro; S Sakota; T Nishimura; H Yoshikawa; M Osame
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

9.  Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome.

Authors:  F P Thomas; R V Lebo; G Rosoklija; X S Ding; R E Lovelace; N Latov; A P Hays
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

10.  Anomalous superficial peroneal nerve and variant cutaneous innervation of the sural nerve on the dorsum of the foot: a case report.

Authors:  Somayaji Nagabhooshana; Venkata Ramana Vollala; Vincent Rodrigues; Mohandas Rao
Journal:  Cases J       Date:  2009-11-18
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