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Molecular genetic analysis of Meesmann's corneal dystrophy

Molecular genetic analysis of Meesmann's corneal dystrophy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200058010
Enrollment
Unknown
Registered
2022-03-26
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Meesmann's corneal dystrophy

Interventions

case series:None

Sponsors

Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meesmann's corneal dystrophy patients and their relatives; 2. Without systemic or ocular genetic diseases; 3. Willing to undergo genetic testing and sign informed consent.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Genetic testing;—

Countries

China

Contacts

Public ContactDai Qi
dq@mail.eye.ac.cn+86 18667127070

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026