French Wilson Disease Registry
Registre Wilson France
Fondation Ophtalmologique Adolphe de Rothschild
1,000 participants
Jan 1, 2005
OBSERVATIONAL
Conditions
Summary
This registry concerns adults and children with Wilson's disease. The collection of a large amount of data will allow a better understanding of the epidemiology of this rare disease, in particular the age of onset according to the hepatic or hepato-neurological forms, but also the geographical distribution of patients consulting in France. This database will also make it possible to know all the therapies prescribed to "Wilsonian" patients. The genetic study of these patients will make it possible to specify the various genetic mutations involved in Wilson's disease. The information (clinical, biological, radiological and genetic) relating to the disease will be entered by a doctor or a professional specialising in Wilson's disease.
Eligibility
Inclusion Criteria1
- All patients suffering from Wilson disease
Exclusion Criteria1
- Lack of written consent from the patient or their legal representative
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
Age, gender, date of diagnosis, clinical symptoms, ethnic charateristics and family tree will be collected and recorded on the Wilson Register during routine clinical care
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05231876