医学
视束
视神经病变
视交叉
视力
Leber遗传性视神经病
眼科
视神经炎
高强度
突变
视神经
磁共振成像
放射科
多发性硬化
遗传学
生物
精神科
基因
作者
Xintong Xu,Huanfen Zhou,Mingming Sun,Yuyu Li,Biyue Chen,Xiyun Chen,Quangang Xu,Patrick Yu‐Wai‐Man,Patrick Yu-Wai-Man,Shihui Wei
标识
DOI:10.1136/bjo-2023-324628
摘要
T2 HS in the pregeniculate visual pathway is a frequent finding in LHON. Signal changes in the OCh/OTr and chiasmal enlargement, in particular within the first 3 months of visual loss, were more commonly seen in patients carrying the m.11778G>A mtDNA mutation, which may be of diagnostic significance.
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