Eeg-Olofsson O, al-Zuhair A G, Teebi A S, al-Essa M M
Department of Paediatrics, Faculty of Medicine, Kuwait University.
Brain Dev. 1988;10(4):260-2. doi: 10.1016/s0387-7604(88)80010-x.
Two girls with Rett syndrome were investigated including muscle biopsy. The electron microscopy study revealed abnormally swollen and dumb-bell shaped mitochondria. Based on the findings of mitochondrial changes it can be assumed that such changes are due to a mitochondrial mutation steered by an X-borne gene mutation. As a result and because the mitochondrial DNA is maternally inherited, the male zygote may not be implanted or it will proceed to an early embryonal death. The mitochondrial changes with the ensuing effects may be the basic cause of the syndrome.
对两名患有雷特综合征的女孩进行了包括肌肉活检在内的检查。电子显微镜研究显示线粒体异常肿胀且呈哑铃状。基于线粒体变化的发现,可以推测这种变化是由X连锁基因突变引发的线粒体突变所致。因此,由于线粒体DNA是母系遗传的,雄性合子可能无法着床,或者会在胚胎早期死亡。线粒体变化及其后续影响可能是该综合征的根本原因。