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Molecular Genetics Study of Marfan Syndrome Family with Wadenberg Syndrome

Molecular Genetics Study of Marfan Syndrome Family with Wadenberg Syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037926
Enrollment
Unknown
Registered
2020-09-04
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-11-16

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

Conditions

Marfan Syndrome

Interventions

case series:Nil

Sponsors

Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All members of the family.

Exclusion criteria

Exclusion criteria: NIl

Design outcomes

Primary

MeasureTime frame
mutant gene;—

Countries

China

Contacts

Public ContactYqiang Huang

Shantou International Eye Center

hyq@jsiec.org+86 15915542805

Outcome results

None listed

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