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[先天性低髓鞘性神经病一例中的施万细胞病理学与轴突减少]

[Schwann cell pathology and axonal reduction in a case of congenital neuropathy with hypomyelinization].

作者信息

Landrieu P, Selva J, Cau D, Barre M, Metral S, Leonard C

出版信息

Arch Fr Pediatr. 1985 Aug-Sep;42(7):497-502.

PMID:4083969
Abstract

A case of congenital dysmyelinating neuropathy is reported, in which computerised morphological analysis showed a prominent loss of fibers with large axons, in addition to overall thinness of myelin sheath. Ultrastructural examination showed aberrant formation of basal lamina and abnormal ensheathment by Schwann cells of both myelinated and unmyelinated fibers. Hypomyelination appears to be only one aspect of this neuropathy, in which axonal pathology plays a major role.

摘要

本文报道了1例先天性脱髓鞘性神经病,计算机形态学分析显示,除髓鞘整体变薄外,大轴突纤维显著缺失。超微结构检查显示,基膜形成异常,有髓和无髓纤维的施万细胞包裹异常。髓鞘形成减少似乎只是这种神经病的一个方面,其中轴突病变起主要作用。

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