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Whole Exome Sequencing and Screening of Pathogenic Genes in Typical Families With Hip Dysplasia

Multiomics sequencing and joint analysis of typical families with DDH

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057975
Enrollment
Unknown
Registered
2022-03-24
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

Developmental dysplasia of the hip

Interventions

None listed

Sponsors

Chinese PLA general hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. In the same family, two or more immediate family members have DDH (clearly diagnosed by two orthopedic surgeons with senior professional titles on imaging); 2. Aged 18-85; 3. Hip joint X-ray screening and peripheral blood sample sampling; 4. Patients voluntarily participated in the study and signed written informed consent.

Exclusion criteria

Exclusion criteria: 1. Imaging examination ruled out DDH diagnosis; 2. Severe diseases of the blood system, such as hemolysis, myelodysplastic syndrome, coagulation related diseases, etc.; 3. There is no healthy control in the immediate family; 4. The researcher considers it inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Statistics of the number of gene mutation sites;Statistical distribution of single nucleotide mutation types;Number statistics and locus distribution of DDH-related susceptible genes;Related molecular pathways and cell component statistics involving mutated genes;

Secondary

MeasureTime frame
Imaging records;DDH typing;

Countries

China

Contacts

Public ContactWei Chai

Chinese PLA general hospital

chaiweiguanjie@sina.com+86 13601372998

Outcome results

None listed

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