Back to Search Start Over

Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation

Authors :
Brian C. Mansfield
Kari H. Branham
Benjamin R. Yerxa
Source :
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

The Foundation Fighting Blindness is a 50‐year old 501c(3) non‐profit organization dedicated to supporting the development of treatments and cures for people affected by the inherited retinal diseases (IRD), a group of clinical diagnoses that include orphan diseases such as retinitis pigmentosa, Usher syndrome, and Stargardt disease, among others. Over $760 M has been raised and invested in preclinical and clinical research and resources. Key resources include a multi‐national clinical consortium, an international patient registry with over 15,700 members that is expanding rapidly, and an open access genetic testing program that provides no cost comprehensive genetic testing to people clinically diagnosed with an IRD living in the United States. These programs are described with particular focus on the challenges and outcomes of establishing the registry and genetic testing program.

Details

ISSN :
15524876 and 15524868
Volume :
184
Database :
OpenAIRE
Journal :
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Accession number :
edsair.doi.dedup.....0d02473cbecc9a1ba41e91822b0324f3
Full Text :
https://doi.org/10.1002/ajmg.c.31825