Ciafaloni E, Santorelli F M, Shanske S, Deonna T, Roulet E, Janzer C, Pescia G, DiMauro S
H. Houston Merritt Clinical Research Center for Muscular Dystrophy and Related Diseases, Columbia-Presbyterian Medical Center, New York, New York.
J Pediatr. 1993 Mar;122(3):419-22. doi: 10.1016/s0022-3476(05)83431-6.
A 6 1/2-year-old girl had developmental regression, and Leigh syndrome was diagnosed. A second girl born to the same mother after heterologous artificial insemination also lost acquired skills and died at 2 1/2 years of age; neuropathologic examination confirmed the diagnosis of Leigh syndrome. Tissues from both children and from the mother had a point mutation at nucleotide 8993 in the adenosinetriphosphatase 6-gene of mitochondrial DNA. This family illustrates that Leigh syndrome can be transmitted by maternal inheritance.
一名6岁半的女孩出现发育倒退,被诊断为 Leigh 综合征。同一母亲在接受异源人工授精后所生的第二个女孩也丧失了已获得的技能,并于2岁半时死亡;神经病理学检查确诊为 Leigh 综合征。两个孩子以及母亲的组织在线粒体DNA的三磷酸腺苷酶6基因的第8993位核苷酸处存在点突变。这个家族表明 Leigh 综合征可通过母系遗传。