摘要
简介:Leber氏视神经遗传性神经病(LHON)是双眼失明的常见原因,目前尚无有效的治疗方法。 1871年,德国眼科医生Theodor Leber率先描述了他的同名疾病的临床特征,经过近百年的不懈努力,研究人员不断加深对LHON的认识。 近年来,利用基因治疗,几个小组在疾病的治疗方面取得了突破性的进展。 结论:在本文中,我们将回顾研究人员面对我们目前对LHON的理解所面临的挑战之旅,并描述LHON从替补到床边的基因治疗研究的转变。
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Current Gene Therapy
Title:The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy
Volume: 17 Issue: 4
关键词:
摘要: Introduction: Leber's Optic Hereditary Neuropathy (LHON) is a common cause of teenaged blindness in both eyes for which there is currently no effective treatment. In 1871, the German ophthalmologist Theodor Leber was the first to describe the clinical characteristics of his namesake disease, and through unremitting efforts over the past 100 years, researchers have continued to increase their understanding of LHON. In recent years, using gene therapy, several groups have obtained breakthroughs in the treatment of the disease.
Conclusion: In this article, we will review the challenging journey that researchers faced towards our current understanding of LHON, and describe the transition of gene therapy research for LHON from the bench to bedside.
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Cite this article as:
The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy, Current Gene Therapy 2017; 17 (4) . https://dx.doi.org/10.2174/1566523218666171129204926
DOI https://dx.doi.org/10.2174/1566523218666171129204926 |
Print ISSN 1566-5232 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5631 |
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