1) pure type mitochondrial myopathy
单纯型线粒体肌病
1.
Objective To investigate the clinical and pathological features of pure type mitochondrial myopathy.
目的 探讨单纯型线粒体肌病的临床和病理特点。
2) Pure mitochondria
单纯线粒体
4) mitochondrial myopathy
线粒体肌病
1.
Chronic progressive external ophthalmoplegia type of mitochondrial myopathy(report of 3 families);
慢性进行性眼外肌瘫痪型线粒体肌病(附3个家系报告)
2.
Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy;
线粒体肌病患者线粒体DNA的突变分析
3.
Mitochondrial myopathy and mitochondrial encephalomyopathy;
线粒体肌病和脑肌病临床及预后的研究
6) 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。
补充资料：眼肌型进行性肌营养不良
眼肌型进行性肌营养不良
又称Kilon与Nevin型"肌营养不良。散发，呈常染色体显性遗传。20岁左右起病。缓慢进展的二侧眼睑下垂，眼球运动障碍，导致眼球固定。诊断较困难，若同时伴有肢体近端肌或口周部肌病症者，有助诊断。
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