2) Mitochondrial encephalopathy-lactic acidosis-stroke like episode
线粒体脑肌病伴乳酸血症和卒中样发作
3) Mitochondrial encephalomyopothy with lactic acidosis and stroke-liked episodes (MELAS syndrome)
线粒体脑肌病伴乳酸血症和卒中样发作(MELAS综合征)
4) Mitochondrial encephalomyopathies
线粒体脑肌病
1.
Mitochondrial encephalomyopathies are a group of multisystemic disorders that caused by Mitochondrial DNA or nuclear mutations to result in disturbance of mitochondrial Structures and function, which involve central nervous system and muscle mainly.
线粒体脑肌病是一组以mtDNA或核DNA(nDNA)突变导致线粒体结构和功能异常,以中枢神经系统和肌肉组织病变为主要表现的多系统疾病。
5) mitochondrial encephalomyopathy
线粒体脑肌病
1.
Clinical,imaging and pathological features of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(report of 1 case)
线粒体脑肌病伴高乳酸血症和脑卒中样发作的临床、影像学及病理学特点(附1例报告)
2.
Analysis of two mitochondrial encephalomyopathy cases on clinical、image and pathology
线粒体脑肌病2例临床、影像及病理分析
6) stroke-like episodes
卒中样发作
1.
Clinical,imaging and pathological features of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(report of 1 case)
线粒体脑肌病伴高乳酸血症和脑卒中样发作的临床、影像学及病理学特点(附1例报告)
补充资料：短暂性脑缺血发作
短暂性脑缺血发作
transient ischemic attack,TIA
急性脑血管病之一。指一时性脑缺血引起的一种局限性脑功能丧失，通常在24小时内完全缓解，不遗留重要神经功能缺陷。主要病因是脑动脉粥样硬化，亦可见于各种原因的动脉炎和心脏病。颈内动脉系统的脑缺血发作以病灶对侧的单瘫或偏瘫为常见，尤以上肢和面部为重，可伴有失语及精神症状。椎-基底动脉系统的脑缺血发作常见症状有眩晕、复视、构音障碍、吞咽困难、共济失调、单侧或双侧肢体瘫痪或感觉障碍等，至少两种以上症状共同出现。大脑后动脉供血不足可出现皮质盲，对侧同向偏盲。防治短暂性脑缺血发作，应针对每个人的病因，对发作次数多，考虑为微栓塞所致者，可慎重地选择抗凝治疗。主要病灶在颈部的动脉、颈内动脉颅内段或限于大脑中动脉主干者，可结合病人的具体情况考虑外科治疗。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条