Suppr超能文献

男子患具有多发性硬化样表现的莱伯遗传性视神经病变。

Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.

机构信息

1Institute of Neurological Sciences, National Research Council, Mangone, Cosenza, Italy.

出版信息

Mult Scler. 2011 Jun;17(6):763-6. doi: 10.1177/1352458511404033.

Abstract

A 35-year-old young man displayed Leber's optic neuropathy (LHON) due to T14484C and multiple sclerosis (MS) phenotype that was dominated by symptoms and signs of spinal cord impairment. Magnetic resonance imaging (MRI) revealed demyelinating lesions extending from D6 to D11 in the spinal cord with gadolinium enhancement, while only three linear demyelinating lesions were seen on brain MRI. In the literature, a major involvement of the spinal cord was already reported in three of four male patients with the 14484 LHON mutation who developed MS, but the reasons of this peculiar association remain unknown, and further research in this area is needed.

摘要

一位 35 岁的年轻男性表现出 Leber 的视神经病变(LHON),其突变类型为 T14484C,同时患有以脊髓损伤症状和体征为主的多发性硬化症(MS)表型。磁共振成像(MRI)显示脊髓内脱髓鞘病变从 D6 延伸至 D11 并伴有钆增强,而脑 MRI 上仅可见三个线性脱髓鞘病变。在文献中,已有报道称,四名患有 LHON 突变的男性患者中有三人出现了 MS,其中主要涉及脊髓,但是这种特殊关联的原因尚不清楚,需要在该领域进行进一步的研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验