History of Finding Genes and Mutations Causing Inherited Retinal Diseases

被引:5
|
作者
Daiger, Stephen P. [1 ]
Sullivan, Lori S. [1 ]
Cadena, Elizabeth L. [1 ]
Bowne, Sara J. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Sch Publ Hlth, Houston, TX 77030 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2024年 / 14卷 / 09期
关键词
RETINITIS-PIGMENTOSA; DOMINANT MUTATION; SEQUENCE VARIANTS; LINKAGE; DYSTROPHY;
D O I
10.1101/cshperspect.a041287
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
This is a brief history of the work by many investigators throughout the world to find genes and mutations causing inherited retinal diseases (IRDs). It largely covers 40 years, from the late-1980s through today. Perhaps the best reason to study history is to better understand the present. The "present" for IRDs is exceptionally complex. Mutations in hundreds of genes are known to cause IRDs; tens of thousands of disease-causing mutations have been reported; clinical consequences are highly variable, even within the same family; and genetic testing, counseling, and clinical care are highly advanced but technically challenging. The aim of this review is to account for how we have come to know and understand, at least partly, this complexity.
引用
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页数:11
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