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Genetic diagnosis of Wilson's disease

Genetic diagnosis of Wilson's disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-DDD-17010552
Enrollment
Unknown
Registered
2017-02-04
Start date
2017-01-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Wilson Disease

Interventions

Gold Standard:Clinical symptoms
Family history of genetic
Plasma ceruloplasmin levels
Urine copper levels of 24 hours
The nervous system of assessment and head imaging examination
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ATP7B

Sponsors

Anhui Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Diagnosed cases of clinical symptoms and copper metabolism

Exclusion criteria

Exclusion criteria: Cases of diagnosis is not clear

Design outcomes

Primary

MeasureTime frame
pregnancy outcome;

Countries

China

Contacts

Public ContactLimin WU

Center for Reproductive Medicine and Prenatal Diagnosis, Anhui Provincial Hospital affiliated to Anhui Medical University

wuliminmail@126.com+86 13605601977

Outcome results

None listed

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