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Identification and functional study of the pathogenic gene of an autosomal dominant inherited family with spondyloepimetaphyseal dysplasis

Identification and functional study of the pathogenic gene of an autosomal dominant inherited family with spondyloepimetaphyseal dysplasis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-17011919
Enrollment
Unknown
Registered
2017-07-09
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-07-17

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

Conditions

spondyloepimetaphyseal dysplasis

Interventions

Case series:No

Sponsors

Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: No

Exclusion criteria

Exclusion criteria: No

Design outcomes

Primary

MeasureTime frame
bone turnover markers;—

Countries

China

Contacts

Public ContactZhenlin Zhang

Shanghai Jiao Tong University Affiliated Sixth People's Hospital

zzl2002@medmail.com.cn+86 13621673716

Outcome results

None listed

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