About this trial
This is a single-centre, observational cohort study with the following objectives: Firstly, the investigators aim to evaluate the vision-related quality of life and mental health status in congenital ectopia lentis patients. Secondly, the investigators target to investigate the correlations between genotype and clinical phenotype in patients of congenital ectopia lentis. Thirdly, to explore the metabolic profiles in the aqueous humor (AH) of patients with congenital ectopia lentis. Lastly, this study aims to explore the longitudinal changes of ocular biological parameters and complications in patients with postoperative congenital ectopia lens in the Chinese population.
Eligibility criteria
Qualifiers
Diagnosed with congenital lens dislocation and age ≥ 3 years old.
Agree to participate in this study with written informed consent from patients or legal guardians.
Disqualifiers
History of ophthalmic trauma or other ophthalmic surgeries.
Combined with other ophthalmic diseases such as primary glaucoma, uveitis and corneal disease.
Patients who could not cooperate in the examinations.
Trial design
Treatments tested in this trial
- Not listed