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Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non‐profit foundation
- 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.
- Subjects :
- Adult
Male
0301 basic medicine
open access genetic testing
medicine.medical_specialty
inherited retinal diseases
Organizations, Nonprofit
Usher syndrome
030105 genetics & heredity
Access to Information
Young Adult
03 medical and health sciences
patient registry
Retinal Diseases
Retinitis pigmentosa
Genetics
medicine
Humans
Genetic Testing
Registries
Genetics (clinical)
Genetic testing
Research Reviews
Patient registry
medicine.diagnostic_test
clinical consortium
business.industry
Research Review
Foundation (evidence)
Non profit
Middle Aged
medicine.disease
venture philanthropy
Stargardt disease
030104 developmental biology
Clinical research
Family medicine
Mutation
Female
business
Subjects
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