Kremer I, Lerman-Sagie T, Mukamel M, Sandbank J, Nissenkorn I, Mimouni M
Department of Ophthalmology, Beilinson Medical Center, Petah Tiqva, Israel.
Ophthalmologica. 1989;199(2-3):106-10. doi: 10.1159/000310025.
Funduscopic and retinal light- and electron-microscopic findings are described in an infant with progressive neurologic deterioration leading to death. Brain autopsy findings were consistent with Leigh's disease. The retinal mitochondria showed marked degenerative changes, the cristae were almost completely destroyed and electron-dense material filled a major part of the cavity. These changes are typically described in the late stages of mitochondrial diseases but have not been described before in retinal mitochondria in a patient with Leigh's disease.
本文描述了一名患有进行性神经功能恶化并最终死亡的婴儿的眼底及视网膜光镜和电镜检查结果。脑部尸检结果符合 Leigh 病。视网膜线粒体显示出明显的退行性变化,嵴几乎完全被破坏,电子致密物质填充了大部分腔隙。这些变化通常在线粒体疾病的晚期出现,但此前尚未在 Leigh 病患者的视网膜线粒体中被描述过。