Possibia

3613948

Last Update Posted: 2021-10-25

Recruiting has ended

All Genders

accepted

4 months-75 Years

280 Estimated Participants

No Expanded Access

Observational Study

Does not accept healthy volunteers

Study on the Effects of Mutations Under Inherited Retinal Disease in Korean

To develop comprehensive genetic maps of inherited retinal diseases in Korean

  • Establishment of comprehensive genetic database in Koreans with inherited retinal diseases including frequently mutated genes, genotype-phenotype correlations, and visual prognosis."

Group/ Cohort Label : Subject with age between 6 months and 65 years who have not receive molecular genetic testing Group / Cohort Description : Consecutive subjects with inherited retinal disease who are willing to do genetic testing using whole exome sequencing (n=265) and whole genome sequencing (n=15) and agree to informed consent of the study

Eligibility

Relevant conditions:

Inherited Retinal Dystrophy Primarily Involving Sensory Retina

Inherited Retinal Dystrophy Primarily Involving Retinal Pigment Epithelium

If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.

locations

Contact Information

Overall Contact

No valid contacts available

Data sourced from ClinicalTrials.gov