构音障碍
内囊
辐射冠(胚胎学)
轻瘫
医学
穿通动脉
冠状面
桥
冲程(发动机)
基底神经节
解剖
梗塞
白质
听力学
心脏病学
放射科
磁共振成像
动脉
中枢神经系统
内科学
心肌梗塞
工程类
卵丘
卵泡
机械工程
激素
作者
Ryutaro Hanyu,Shintaro Tsuboguchi,Itaru Ninomiya,Takanobu Ishiguro,Takuya Konno,Masato Kanazawa,Osamu Onodera
标识
DOI:10.1016/j.jns.2022.120456
摘要
Pure dysarthria-facial paresis is a rare stroke syndrome, primarily caused by lesions in the cortical or subcortical bulbar motor area, corona radiata, basal ganglia, internal capsule, and pons [1]. Corona Radiata is supplied by the lenticulostriate arteries (LSAs), long insular arteries (LIAs), and white matter medullary arteries (WMMAs); however, LSA infarctions are the most common [2]. We encountered four cases of dysarthria-facial paresis syndrome and found clear evidence of LIA and WMMA infarctions on coronal images.
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