Hussain Rehan M, Tran Kimberly D, Maguire Albert M, Berrocal Audina M
Ophthalmic Surg Lasers Imaging Retina. 2019 Oct 1;50(10):661-663. doi: 10.3928/23258160-20191009-01.
Leber's congenital amaurosis (LCA) is a rare inherited retinal degeneration (IRD) that causes severe vision loss, nyctalopia, and nystagmus within the first few years of life. RPE65 gene mutations cause approximately 6% of LCA cases and have become the target for therapy since voretigene neparvovec-rzyl became the first U.S. Food and Drug Administration-approved gene therapy product for IRDs in 2017. The surgery involves pars plana vitrectomy with subretinal injection of a viral vector that carries a functional copy of the RPE65 gene. Intraoperative optical coherence tomography is a useful adjunctive tool to confirm the injection has reached the subretinal space.
莱伯先天性黑蒙(LCA)是一种罕见的遗传性视网膜变性(IRD),在生命的最初几年会导致严重视力丧失、夜盲和眼球震颤。RPE65基因突变导致约6%的LCA病例,自2017年voretigene neparvovec-rzyl成为美国食品药品监督管理局批准的首个用于IRD的基因治疗产品以来,RPE65基因突变已成为治疗靶点。该手术包括玻璃体平坦部切除术及视网膜下注射携带RPE65基因功能拷贝的病毒载体。术中光学相干断层扫描是一种有用的辅助工具,可用于确认注射已到达视网膜下间隙。