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先天性髓鞘形成不足和过度髓鞘形成神经病。两例报告。

Congenital hypo- and hypermyelination neuropathy. Two cases.

作者信息

Vallat J M, Gil R, Leboutet M J, Hugon J, Moulies D

机构信息

Department of Neurology, University Hospital, Limoges, France.

出版信息

Acta Neuropathol. 1987;74(2):197-201. doi: 10.1007/BF00692853.

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.

摘要

最近有两名年轻患者因腓骨肌萎缩综合征前来作者处接受检查。由于最初症状在婴儿期就已出现,怀疑是先天性髓鞘形成不足性神经病,并对腓浅神经进行了活检。观察到严重且广泛的脱髓鞘/再髓鞘化迹象。这些特征在形态学上与在球状或腊肠样神经病中观察到的特征相似。文中讨论了髓鞘过度形成的机制。

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