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Leber遗传性视神经病变中的白质改变:MRI表现

White matter changes in Leber's hereditary optic neuropathy: MRI findings.

作者信息

Küker W, Weir A, Quaghebeur G, Palace J

机构信息

Department of Neuroradiology, The Radcliffe Infirmary, Oxford, UK.

出版信息

Eur J Neurol. 2007 May;14(5):591-3. doi: 10.1111/j.1468-1331.2007.01757.x.

DOI:10.1111/j.1468-1331.2007.01757.x
PMID:17437624
Abstract

Leber's hereditary optic neuropathy is a mitochondrial disorder causing bilateral optic nerve degeneration. It is sometimes associated with clinical signs of multiple sclerosis. We report MRI findings in two patients with LHON-MS and comment on possible distinguishing features of this disease entity.

摘要

莱伯遗传性视神经病变是一种导致双侧视神经变性的线粒体疾病。它有时与多发性硬化症的临床症状相关。我们报告了两名患有莱伯遗传性视神经病变合并多发性硬化症(LHON-MS)患者的MRI检查结果,并对这种疾病实体可能的鉴别特征进行了评论。

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