Study of inherited eye conditions in families
Part of Eyes & vision clinical trials.
This study looks at families who have inherited (passed down) eye conditions, using eye exams and blood tests. It may help researchers understand what causes these conditions and find better ways to diagnose them.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Be 4 years of age or older
- Be able to understand and agree to the study (or have consent as allowed by the study)
- Have a family member with an inherited eye disease
- Be able to cooperate with eye exams and blood draws
- Not have another condition that can look like inherited eye disease
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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This study uses whole exome and whole genome genetic tests to look for DNA changes linked to inherited or congenital eye problems. It may help families and doctors better understand the cause of the eye condition and guide future care.
This study observes people with various eye conditions to understand how they progress and to help improve future treatments. It may help you learn more about your condition and contribute to medical knowledge.
This study collects DNA samples and medical information from people with rare inherited eye diseases and their close relatives. The goal is to learn more about the genetic causes of these conditions and improve diagnosis and care.
This study is a registry, meaning it collects information about people with inherited retinal (retina) diseases. It may help researchers learn how these conditions progress and connect you with future studies or treatments.
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