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一名患有瓦登伯革氏综合征的患者出现的一种罕见的脱髓鞘性神经病。

An unusual demyelinating neuropathy in a patient with Waardenburg's syndrome.

作者信息

Jacobs J M, Wilson J

机构信息

Department of Neuropathology, Institute of Neurology, London, UK.

出版信息

Acta Neuropathol. 1992;83(6):670-4. doi: 10.1007/BF00299420.

Abstract

We present clinical and laboratory data from a patient with Waardenburg's syndrome type II comprising iris heterochromia and deafness, complicated by Hirschsprung's disease--a known association--and an unusual demyelinating peripheral neuropathy--a unique association. The neuropathy is characterised by excessive focal folding of myelin sheaths. It is our view that, although both disorders could represent the consequences of neural crest embryopathy, it is more likely that they are associated by chance.

摘要

我们报告了一名患有II型瓦登伯革氏综合征患者的临床和实验室数据,该患者伴有虹膜异色症和耳聋,并并发先天性巨结肠(一种已知的关联疾病)以及一种罕见的脱髓鞘性周围神经病(一种独特的关联疾病)。这种神经病的特征是髓鞘过度局灶性折叠。我们认为,虽然这两种疾病都可能代表神经嵴胚胎病的后果,但它们更有可能是偶然相关的。

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