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Detection of WFS1 gene mutations in Chinese subjects with Wolfram syndrome

Functional characterization of WFS1 gene mutations in Chinese Wolfram syndrome

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017261
Enrollment
Unknown
Registered
2018-07-20
Start date
2018-08-01
Completion date
Unknown
Last updated
2018-08-27

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

Conditions

Wolfram syndrome

Interventions

Cases:Nil

Sponsors

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

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with Wolfram syndrome who have clinical manifestations of diabetes, diabetes, optic atrophy and deafness.

Exclusion criteria

Exclusion criteria: No

Design outcomes

Primary

MeasureTime frame
WFS1 gene sequence analysis;—

Countries

Chian

Contacts

Public ContactQichen Fang

Shanghai Jiao Tong University Affiliated Sixth People's Hospital

fqichen@163.com+86 18930172847

Outcome results

None listed

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