Identification and Verification of Candidate Genes Responsible for Optic Disc Drusen
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Optic Disk Drusen
- Sponsor
- Copenhagen University Hospital at Herlev
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Candidate gene
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The goal of this observational study is to learn about the genetic background for the development of optic disc drusen. The main question is:
• Can one or more candidate genes be found?
Participants will have a blood sample taken and answer a questionnaire.
Detailed Description
The study is an international collaboration between University of Utah, University of Sydney, University of Valladolid, and University of Copenhagen. Patients with Optic disc drusen from 15 known optic disc drusen-families from different countries (USA, Australia, Spain and Denmark) are participating in this study. Blood samples are drawn from each patient and their affected and unaffected family members, and DNA will be extracted. The investigators will do an Optical coherence tomography-scan (according to ODDS Consortium guidelines), and the participant will be asked to fill out the Visual Function Questionnaire (VFQ-25) including four additional questions about optic disc drusen. The etiology of optic disc drusen will be analyzed with a Whole Exome Sequencing (WES), with the use of Next Generation Sequencing (NGS). Prior to WES, all participants will receive genetic counseling by a consultant to ensure awareness of possible secondary genetic findings.
Investigators
Alvilda Steensberg
Principal Investigator
Rigshospitalet, Denmark
Eligibility Criteria
Inclusion Criteria
- •Adult patients over the age of 18, who are capable of giving consent
- •Diagnosis of optic disc drusen and a minimum of 3 optic disc drusen-affected family members
Exclusion Criteria
- •Less than 3 affected family members
- •Under the age of 18 or mentally disabled
Outcomes
Primary Outcomes
Candidate gene
Time Frame: 2023-2024
Genetics variants shared by the families will be compared with findings in the remaining families and identical genes will undergo further analysis.