Clinical and Molecular Analysis of Genetic Eye Disorders
- Investigator Initiated
- Principal Investigator: Terri Young, MD, MBA, FARVO
- Study Coordinator: Nickie Stangel
Study objective:
To identify the gene or genes responsible for developmental causes of blindness in the world, and to establish a Pediatric Ophthalmic Genetics and Research Program at the University of Wisconsin – Madison.
Study design:
One study visit involving a medical history questionnaire, ophthalmic evaluations, and a blood/saliva sample for genetic/DNA analysis.
Inclusion criteria:
- Male or female patients of any age (including minors) who have an ophthalmic disorder that could have a genetic component
- Family members (including minors) of a patient who has an ophthalmic disorder that could have a genetic component
Exclusion criteria:
- Known genetic mutation supporting the clinically diagnosed eye condition