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Detection and analysis of KRT12 gene mutation in a single family with Meesmann corneal dystrophy

Detection and analysis of KRT12 gene mutation in a single family with Meesmann corneal dystrophy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101856
Enrollment
Unknown
Registered
2025-04-30
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-05-05

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

Observation group:None

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meesmann's corneal dystrophy patients and their relatives who have received genetic testing and signed informed consent. 2. No systemic or other ocular hereditary diseases.

Exclusion criteria

Exclusion criteria: 1. Other types of corneal dystrophy patients; 2. Accompanied by systemic or other ocular hereditary diseases. 3. Meesmann's corneal dystrophy patients or relatives who have not received genetic testing.

Design outcomes

Primary

MeasureTime frame
DNA;—

Countries

China

Contacts

Public ContactDai Qi

Eye Hospital Affiliated to Wenzhou Medical University

dq@mail.eye.ac.cn+86 571 88185666

Outcome results

None listed

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