Literature DB >> 7687811

Degeneration of anterior horn cell in neuronal type of Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type II): a Golgi study.

S Ono1, K Hara, H Sasaki, I Sugano, K Nagao.   

Abstract

A morphological study using the Golgi impregnation method was carried out on the anterior horn cells at cervical (C), thoracic (Th), and lumbar (L) levels of the spinal cord in a patient with neuronal type of Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type II) and an age-matched control. The present study demonstrated an uneven cell body surface, loss of cells (particularly large cells), loss of dendrites, reduced dendritic extent and an irregular surface and shape of dendrites at the C and L levels. In contrast, hematoxylin and eosin and Klüver-Barrera staining showed only simple atrophy or no change. The Th level of the patient showed none of these changes. Our results suggest that the degeneration or loss of dendrites of anterior horn cells by the Golgi staining method, which is most severe at the L level, is closely related to clinical findings such as muscle atrophy and weakness in neuronal type of Charcot-Marie-Tooth disease.

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Year:  1993        PMID: 7687811     DOI: 10.1007/bf00334668

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


  17 in total

1.  Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

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Journal:  Arch Neurol       Date:  1968-06

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Authors:  J Julien; C Vital; J M Vallat; M Coquet; M Le Blanc
Journal:  Nouv Presse Med       Date:  1974-01-19

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Authors:  M E Scheibel; T L Davies; R D Lindsay; A B Scheibel
Journal:  Exp Neurol       Date:  1974-02       Impact factor: 5.330

4.  Contribution to the quantitative study of the nervous tissue. A new method for measurement of the volume and surface area of neurons.

Authors:  H Mannen
Journal:  J Comp Neurol       Date:  1966-01       Impact factor: 3.215

5.  Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family.

Authors:  J Berciano; O Combarros; J Figols; J Calleja; A Cabello; I Silos; F Coria
Journal:  Brain       Date:  1986-10       Impact factor: 13.501

6.  Pathology of peroneal muscular atrophy (Charcot-Marie-Tooth disease).

Authors:  J T Hughes; B Brownell
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-10       Impact factor: 10.154

7.  Hereditary motor and sensory neuropathy type II with axonal lesions.

Authors:  J Julien; C Vital; A Lagueny; X Ferrer
Journal:  J Neurol       Date:  1988-03       Impact factor: 4.849

8.  The clinical features of hereditary motor and sensory neuropathy types I and II.

Authors:  A E Harding; P K Thomas
Journal:  Brain       Date:  1980-06       Impact factor: 13.501

9.  Charcot-Marie-Tooth disease associated with hypertrophic neuropathy: a neuropathologic study of two cases.

Authors:  T W Smith; J Bhawan; R B Keller; U DeGirolami
Journal:  J Neuropathol Exp Neurol       Date:  1980-07       Impact factor: 3.685

10.  Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.

Authors:  R A Ouvrier; J G McLeod; G J Morgan; G A Wise; T E Conchin
Journal:  J Neurol Sci       Date:  1981-08       Impact factor: 3.181

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