Leber遗传性视神经病变中的视力丧失与对称性基底节病变

Vision Loss and Symmetric Basal Ganglia Lesions in Leber Hereditary Optic Neuropathy.

作者信息

Mercuri Matthew A, White Halina, Oliveira Cristiano

机构信息

Departments of Neurology (MAM, HW) and Ophthalmology (CO), Weill Cornell Medical College, New York, New York.

出版信息

J Neuroophthalmol. 2017 Dec;37(4):411-413. doi: 10.1097/WNO.0000000000000524.

DOI:10.1097/WNO.0000000000000524

PMID:28459737

Abstract

A 30-year-old woman with progressive vision loss was found to have asymptomatic, bilateral, and symmetric basal ganglia lesions on MRI and was later diagnosed with Leber hereditary optic neuropathy (LHON). The rare occurrence of basal ganglia changes on MRI in patients with LHON is discussed.

摘要

一名30岁进行性视力丧失的女性在MRI上被发现有双侧对称、无症状的基底节病变，随后被诊断为Leber遗传性视神经病变（LHON）。本文讨论了LHON患者MRI上罕见的基底节改变。