KCT0003061
Completed
未知
Study on the effects of mutations under inherited retinal disease in Korean
ConditionsDiseases of the eye and adnexa
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Diseases of the eye and adnexa
- Sponsor
- Yonsei University
- Enrollment
- 560
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Inherited retinal disease
- •2\) Age between 4 months and 75 years
- •3\) Subject who has clinically confirmed visual impairment including night blindness or photophobia. Subject should meet one of the following criteria
- •\- pigmentary retinopathy in both eyes
- •\- reduced response in photopic or scotopic electroretinogram in both eyes
- •\- photoreceptor degeneration in optical coherence tomography in both eyes
Exclusion Criteria
- •1\) unilateral retinal disease
- •2\) Subject who had previously confirmed genetic testing
- •3\) Age less than 4 months or more than 75 years
- •4\) When congenital infection or trauma are suspicious for the cause of retinal disease
- •5\) When age\-related macular degeneration, myopic degeneration, autoimmune origin are suspicious for the cause of retinal disease
- •6\) No visual impairment or normal electroretinogram (e.g., benign fleck)
- •7\) Illiterate subject who can not understand informed consent
- •8\) Foreigners
Outcomes
Primary Outcomes
Not specified
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