FindTrial
Sign In

Phenotype identification and genetic analysis of congenital syndactyly

Phenotype identification and genetic analysis of congenital syndactyly

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027329
Enrollment
Unknown
Registered
2019-11-09
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-11-11

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

Conditions

syndactyly

Interventions

Case Series:N/A

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 99 Years

Inclusion criteria

Inclusion criteria: 1. Isolated primary hereditary syndactyly; 2. Other relatives in the line of similar lesions.

Exclusion criteria

Exclusion criteria: The family declined to participate in the study.

Design outcomes

Primary

MeasureTime frame
gene;—

Countries

China

Contacts

Public ContactXiang Bo

West China Hospital, Sichuan University

Aygd9680@qq.com+86 18980602116

Outcome results

None listed

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