Gerbitz K D, Obermaier-Kusser B, Zierz S, Pongratz D, Müller-Höcker J, Lestienne P
Institut für Klinische Chemie und Forschergruppe Diabetes, Städtisches Krankenhaus, München, Schwabing, Federal Republic of Germany.
J Neurol. 1990 Feb;237(1):5-10. doi: 10.1007/BF00319660.
Genomic Southern analysis of muscle mitochondrial (mt) DNA from 16 patients with mitochondrial myopathies was performed; 14 of 16 patients had chronic progressive external ophthalmoplegia (CPEO), while 2 patients had mitochondrial myopathies without CPEO. Eleven patients with CPEO, including 5 who exhibited the complete triad of symptoms characteristic of the Kearns-Sayre syndrome (i.e. CPEO, retinal degeneration and heart block) had heteroplasmic mtDNA with deletions ranging from 2.0 to 8.0 kb in length. There was no clear-cut correlation between the size and location of the deletions, on the one hand, and the histochemical and biochemical data or the severity of the disease, on the other.
对16例线粒体肌病患者的肌肉线粒体(mt)DNA进行了基因组Southern分析;16例患者中有14例患有慢性进行性眼外肌麻痹(CPEO),而2例患者患有无CPEO的线粒体肌病。11例CPEO患者,包括5例表现出Kearns-Sayre综合征典型三联征症状(即CPEO、视网膜变性和心脏传导阻滞)的患者,其异质性mtDNA存在长度从2.0到8.0 kb不等的缺失。一方面,缺失的大小和位置与另一方面的组织化学和生化数据或疾病严重程度之间没有明确的相关性。