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Family investigation and pathogenic gene detection of congenital atlantoaxial dislocation

Family investigation and pathogenic gene detection of congenital atlantoaxial dislocation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000041488
Enrollment
Unknown
Registered
2020-12-27
Start date
2021-01-31
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

congenital atlantoaxial dislocation

Interventions

case series:Nil

Sponsors

Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 78 Years

Inclusion criteria

Inclusion criteria: 25 members of the patient's family.

Exclusion criteria

Exclusion criteria: Nil

Design outcomes

Primary

MeasureTime frame
Gene testing;

Countries

China

Contacts

Public ContactQing Wang

Affiliated Hospital of Southwest Medical University

wqspine@163.com+86 13982473000

Outcome results

None listed

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