Genetics of Primary Inherited Disorders of the Optic Nerve: Clinical Applications

被引:27
作者
Allen, Keri F. [1 ]
Gaier, Eric D. [1 ]
Wiggs, Janey L. [1 ]
机构
[1] Harvard Univ, Massachusetts Eye & Ear Infirm, Sch Med, Boston, MA 02114 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2015年 / 5卷 / 07期
关键词
TENSION GLAUCOMA PATIENTS; AXENFELD-RIEGER SYNDROME; CONGENITAL GLAUCOMA; CYP1B1; MUTATIONS; MOUSE MODEL; NEUROPATHY; SPECTRUM; PREVALENCE; THERAPY; FOXC1;
D O I
10.1101/cshperspect.a017277
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Inherited disorders of the optic nerve significantly impact vision in children and adults. The optic nerve disorders most commonly encountered clinically are glaucoma and primary optic neuropathy including Leber's hereditary optic neuropathy (LHON) and autosomal dominant or Kjer's optic atrophy. Current knowledge of the genetics of optic neuropathy and glaucoma makes it possible to test for mutations in disease-causing genes allowing for presymptomatic testing and risk assessment, and recent advances have revealed important disease mechanisms that may suggest potential therapeutic targets. In this perspective, we describe the current approaches and limitations to genetic testing for these disorders and provide an update on the development of gene-based therapies.
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页数:10
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