Bautista J, Muñoz-Málaga A, Chinchón I, Segura D, Salazar J A, Bescansa E, Campos Y, Arenas J
Servicio de Neurología, Hospital Universitario Virgen del Rocío, Sevilla.
Neurologia. 1995 Oct;10(8):319-23.
Four adults with proximal myopathy of mitochondrial origin but no ocular involvement are presented. Biochemical analysis showed combined complex III and IV deficits in the respiratory chain in all cases, suggesting an apparent correlation between clinical phenotype and biochemical findings. Mitochondrial DNA analysis of muscle from 1 patient failed to detect either large-scale deletion or point mutations at position 3243 of tRNA(Leu(UUR)) or at 8344 of tRNA(Lys). The tissue specificity of the disease and the absence of family history suggest that a mutation in a nuclear DNA gene encoding a specific subunit of muscle could underlie this disease.
本文报告了4例成年线粒体起源近端肌病患者,均无眼部受累。生化分析显示,所有病例呼吸链中复合酶Ⅲ和Ⅳ均有缺陷,提示临床表型与生化结果之间存在明显相关性。对1例患者肌肉进行线粒体DNA分析,未检测到tRNA(Leu(UUR)) 3243位或tRNA(Lys) 8344位的大规模缺失或点突变。该疾病的组织特异性及无家族史提示,编码肌肉特异性亚基的核DNA基因突变可能是该病的病因。