脂质沉积性肌病是一种肌细胞内脂肪异常沉积引起的常染色体隐性遗传病。
Lipid storage myopathy is one kind of autosomal recessive inherited disease with lipid abnormally sludging in the muscle cell.
分析该病可能是一种线粒体肌病，属脂质沉积性肌病。
We thought that the "white-body" disease should be one of mitochondrial myopathy, was lipid storage myopathy.
方法择取脂质沉积性肌病伴血清肌酶明显升高的病人14例，将临床表现、血清肌酶、肌电图和肌肉病理及肌肉组织化学改变进行总结分析。
Methods 14 cases of LSM with high level of CK in serum were analyzed clinically and compared with their muscle morphological and histochemical changes.
目的分析3例被误诊的脂质沉积性肌病的临床及病理特点，探讨脂质沉积性肌病被误诊的原因。
Objective to study the clinical and pathological features of 3 cases of misdiagnosised lipid storage myopathy (LSM), and further discover the reasons of diagnosis error in this disease.
目的分析3例被误诊的脂质沉积性肌病的临床及病理特点，探讨脂质沉积性肌病被误诊的原因。
Objective to study the clinical and pathological features of 3 cases of misdiagnosised lipid storage myopathy (LSM), and further discover the reasons of diagnosis error in this disease.
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