Hereditary retinal diseases
Conditions
Interventions
Observation group:None
Sponsors
Eye Hospital Affiliated to Wenzhou Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The target population of this study consists of children with a significant family history of common congenital eye diseases, such as congenital cataract, congenital glaucoma, albinism, persistent primary vitreous proliferation, Stargardt disease, and pathological myopia, including the probands and at least three generations of direct family members. The underage participants in the study obtained the consent of their parents and signed the informed consent form.
Exclusion criteria
Exclusion criteria: Cannot cooperate with clinical examinations; Other family members do not agree to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gene mutation; | — |
Countries
China
Contacts
Public ContactJie Chen
Eye Hospital Affiliated to Wenzhou Medical University
Outcome results
None listed