Literature DB >> 6280438

The peripheral neuropathy in De Sanctis-Cacchione syndrome. Histological, ultrastructural, and morphometric studies.

N Fukuhara, T Kumamoto, H Takasawa, T Tsubaki, Y Origuchi.   

Abstract

Histological, ultrastructural, and morphometric studies were performed on nerve and muscle biopsies from three patients with de Sanctis-Cacchione syndrome. Sural nerves showed marked loss of the myelinated fibers, in proportion to decrease in nerve conduction velocities and in inverse proportion to the severity of the clinical symptoms, which were related to the survival length. The larger fibers were involved earlier and more markedly than the smaller. The unmyelinated fibers were also decreased in number. Electron-microscopic studies showed the presence of primary degeneration of myelin sheaths or Schwann cells. Muscle biopsies showed grouping of type I and type II fibers in all three patients. Therefore, peripheral nerve involvement in de Sanctis-Cacchione syndrome was suggested to result from chronic degeneration of the neuronal cells and Schwann cells.

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Year:  1982        PMID: 6280438     DOI: 10.1007/bf00690635

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


  14 in total

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  1 in total

1.  The influence of DNA repair on neurological degeneration, cachexia, skin cancer and internal neoplasms: autopsy report of four xeroderma pigmentosum patients (XP-A, XP-C and XP-D).

Authors:  Jin-Ping Lai; Yen-Chun Liu; Meghna Alimchandani; Qingyan Liu; Phyu Phyu Aung; Kant Matsuda; Chyi-Chia R Lee; Maria Tsokos; Stephen Hewitt; Elisabeth J Rushing; Deborah Tamura; David L Levens; John J Digiovanna; Howard A Fine; Nicholas Patronas; Sikandar G Khan; David E Kleiner; J Carl Oberholtzer; Martha M Quezado; Kenneth H Kraemer
Journal:  Acta Neuropathol Commun       Date:  2013-05-08       Impact factor: 7.801

  1 in total

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