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水平性眼球运动麻痹伴进行性脊柱侧凸和皮质下梗死患者出现对侧卒中。

Ipsilateral stroke in a patient with horizontal gaze palsy with progressive scoliosis and a subcortical infarct.

机构信息

MRCP, Registrar, Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital Campus, 11 Jalan Tan Tock Seng, Singapore 308433.

出版信息

Stroke. 2011 Jan;42(1):e1-3. doi: 10.1161/STROKEAHA.110.591271. Epub 2010 Nov 18.

Abstract

BACKGROUND AND PURPOSE

horizontal gaze palsy with progressive scoliosis (HGPPS) is a rare congenital disorder caused by mutation in the ROBO3 gene. It is characterized by absent horizontal eye movements with progressive scoliosis developing in childhood and adolescence. To our knowledge, both diffusion tensor imaging evaluation in HGPPS patients who present with stroke and truncating stop codon mutation in the ROBO3 gene have yet to be reported.

SUMMARY OF CASE

we present a man with HGPPS who experienced a left pure motor stroke as a result of a left corona radiata infarct on diffusion-weighted imaging. Diffusion tensor imaging tractography confirmed the presence of uncrossed corticospinal tracts, accounting for the ipsilateral deficit. He was also found to possess a novel ROBO3 stop codon mutation on genetic testing.

CONCLUSIONS

patients with HGPPS may present with stroke symptoms on the ipsilateral side of the infarct in view of uncrossed corticospinal tracts. Truncating mutation in ROBO3 may provide additional pathophysiologic insights.

摘要

背景与目的

水平性眼球麻痹伴进行性脊柱侧凸(HGPPS)是一种由 ROBO3 基因突变引起的罕见先天性疾病。其特征是在儿童和青少年时期出现水平眼球运动缺失和进行性脊柱侧凸。据我们所知,在表现为中风的 HGPPS 患者中以及在 ROBO3 基因中存在截断终止密码子突变的情况下,尚未对弥散张量成像评估进行报道。

病例总结

我们介绍了一位 HGPPS 男性患者,由于左侧放射冠梗死,在弥散加权成像上出现左侧纯运动性中风。弥散张量成像示踪证实存在未交叉皮质脊髓束,导致同侧缺损。在基因检测中,他还发现了一种新的 ROBO3 终止密码子突变。

结论

由于未交叉的皮质脊髓束,HGPPS 患者可能会出现梗死对侧的中风症状。ROBO3 的截断突变可能提供了额外的病理生理学见解。

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