Wheeler Joshua, Hauser Michael A, Afshari Natalie A, Allingham R Rand, Liu Yutao
Center for Human Genetics, Department of Medicine, Duke University Medical Center, Durham, NC, USA 27710.
Reprod Syst Sex Disord. 2012 Jun 3(Suppl 6). doi: 10.4172/2161-038X.S6-001.
Keratoconus is the most common ectatic disorder of the corneal. Genetic and environmental factors may contribute to its pathogenesis. The focus of this article is to summarize current research into the complex genetics of keratoconus. We discuss the evidence of genetic etiology including family-based linkage studies, twin studies, genetic mutations, and genome-wide association studies. The genes implicated potentially include , , , , and Besides the coding mutations, we also highlight the potential contribution of DNA copy number variants in the pathogenesis of keratoconus. Finally, we present future directions for genetic research in the understanding of the complex genetics of keratoconus and its clinical significance. As new functional, candidate genes for keratoconus are being discovered at a rapid pace, the molecular genetic mechanisms underlying keratoconus pathogenesis will advance our understanding of keratoconus and promote the development of a novel therapy.
圆锥角膜是最常见的角膜扩张性疾病。遗传和环境因素可能导致其发病机制。本文的重点是总结目前对圆锥角膜复杂遗传学的研究。我们讨论了遗传病因的证据,包括基于家系的连锁研究、双胞胎研究、基因突变和全基因组关联研究。潜在涉及的基因可能包括 、 、 、 、 和 。除了编码突变外,我们还强调了DNA拷贝数变异在圆锥角膜发病机制中的潜在作用。最后,我们提出了遗传研究的未来方向,以了解圆锥角膜的复杂遗传学及其临床意义。随着圆锥角膜新的功能性候选基因被迅速发现,圆锥角膜发病机制的分子遗传机制将增进我们对圆锥角膜的理解,并促进新疗法的开发。