Literature DB >> 2983258

Heterogeneity of congenital motor and sensory neuropathies.

J Lütschg, F Vassella, E Boltshauser, K Dias, C Meier.   

Abstract

Six children suffering from a congenital motor and sensory neuropathy (CMSN) are described. Severe muscle hypotonia, areflexia and a delay of motor development are detectable in all of them. Sural nerve biopsies exhibited an almost complete absence of myelinated fibres and a correspondingly slow nerve conduction velocity (NCV) of less than 10 m/s was detectable in four patients. A few segments with hypermyelination adjacent to gross hypomyelination were seen in the fifth patient, and the NCV was 15 m/s. The sural nerve of the sixth patient showed a loss of thick myelinated nerve fibres, and his NCV was 25 m/s. These results demonstrate the histological heterogeneity of CMSN which was already detected by the NCV. The relation of our findings to the classification of HMSN by Dyck and Lambert (1968) is discussed.

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Year:  1985        PMID: 2983258     DOI: 10.1055/s-2008-1052541

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  3 in total

1.  MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.

Authors:  N Tachi; N Kozuka; K Ohya; S Chiba; M Naganuma
Journal:  Neuroradiology       Date:  1995-08       Impact factor: 2.804

Review 2.  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

3.  Autosomal recessive hypermyelinating neuropathy.

Authors:  M Sabatelli; T Mignogna; G Lippi; S Servidei; G Manfredi; E Ricci; E Bertini; M Lo Monaco; P Tonali
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

  3 in total

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