Bardet-Biedl Syndrome Study: Clinical and Genetic Epidemiology Study in Adults

Clinical Trial

NCT00213811 Completed

Bardet-Biedl Syndrome Study: Clinical and Genetic Epidemiology Study in Adults.

Observational

Disease

Disease type

Bardet-Biedl

Hereditary retinal disease

Retinitis Pigmentosa

Orphan drug recognition

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

01/06/2003

Closing date

21/09/2005

Inclusion criteria :

Exclusion criteria :

Funding

public

Members involved

Main investigators

Pr Hélène Dollfus

Representative

France

Anterior Segment Rare Eye Diseases (WG4), CPMS & Digital Medecine (TWG10), Epag, ERN-EYE Coordinating committee, Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), National Integration (TWG9), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)

Working Group Leader