高中高半胱氨酸血症和methylenetetrahydrofolate reductase基因多态性(c677t)影后的脑血管性パーキンソニズム1例

Kenju Hara, Keigo Onda, Haruka Ouchi, Ken Shibano, Hideaki Ishiguro
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引用次数: 0

摘要

患者男,56岁,有6年行走困难病史,经帕金森临床表现、锥体征及多发腔隙性脑梗死MRI检查,诊断为血管性帕金森病。虽然他没有高血压,但他有高同型半胱氨酸血症和纯合亚甲基四氢叶酸还原酶(MTHFR)基因变异(C677T)作为缺血性卒中的危险因素。最近的研究表明,高同型半胱氨酸血症和MTHFR基因变异与小血管疾病相关,这表明这些危险因素可能是血管性帕金森病的基础,特别是在没有高血压的患者和发病年龄相对较年轻的患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
高ホモシステイン血症とmethylenetetrahydrofolate reductase遺伝子多型(C677T)をみとめた脳血管性パーキンソニズムの1例
: A 56-year-old man, who presented with 6 years history of difficulty in walking, was diagnosed as having vascular parkinsonism on the basis of the clinical findings of parkinsonism, pyramidal sign and the brain MRI findings of multiple lacunar infarction. Although he did not have hypertension, he had hyperhomocysteinemia and homozygous methylenetetrahydrofolate reductase (MTHFR) gene variant (C677T) as risk factors for ischemic stroke. Recent studies have shown that hyperhomocysteinemia and MTHFR gene variant are associated with small-vessel disease, suggesting that these risk factors may underlie vascular parkinsonism, particularly in patients lacking hypertension and in those with a relatively younger age at onset of this disease.
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