角膜病
医学
角膜移植
遗传增强
治疗方式
眼科
移植
内皮功能障碍
营养不良
角膜营养不良
外科
角膜
病理
生物
遗传学
内科学
基因
作者
Yu Qiang Soh,Gary S. L. Peh,Jodhbir S. Mehta
出处
期刊:Regenerative Medicine
[Future Medicine]
日期:2018-01-01
卷期号:13 (1): 97-115
被引量:24
标识
DOI:10.2217/rme-2017-0081
摘要
Fuchs’ endothelial dystrophy (FED) is characterized by corneal endothelial dysfunction and guttate excrescences on the posterior corneal surface, and is the leading indication for corneal transplantation in developed countries. In severe cases, keratoplasty is considered as the gold standard of treatment. However, there have been significant developments in our understanding of FED over the past decade. Attempts have been made to treat this disease with regenerative therapy techniques such as primary descemetorhexis without an endothelial graft or with a tissue-engineering approach. The discovery of a strong association between the CTG18.1 trinucleotide repeat expansion sequence and FED may pave the way for gene therapy strategies in the future. In this review, we evaluate these novel therapeutic modalities as possible alternatives to keratoplasty as the standard of care for FED.
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