Clinical Trial
Disease
Disease type
Keratoconus
Patient type
Adult
Children
Inclusion / Exclusion
Funding
Private
Members involved
Others investigators
Pr Bart LEROY
Representative
Belgium
Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), National Integration (TWG9), Research (TWG8), Retinal Rare Eye Diseases (WG1)
Working Group Leader
Pr Elfride DE BAERE
Substitute
Belgium
Genetic Diagnostics (TWG6), Retinal Rare Eye Diseases (WG1)
Working Group Leader
Pr Pierre FOURNIE
Representative
France
Anterior Segment Rare Eye Diseases (WG4), Registries & Epidemiology (TWG7), Research (TWG8)
Dr João Pedro Marques
Substitute
Portugal
National Integration (TWG9), Research (TWG8), Retinal Rare Eye Diseases (WG1)
ERN EYE member investigating site
HCP : Principal investigators
Ghent University Hospital, Ghent, Belgium
Adress
Corneel Heymanslaan 10
9000 Ghent
Belgium
University Hospitals Leuven, Belgium
Adress
Herestraat 49
3000 Leuven
Belgium
Reference Center Rare Diseases ‘Genetic Sensory Diseases’, MAOLYA, Montpellier, France
Adress
Hôpital Gui de ChauliacService Ophtalmologie80, avenue Augustin Fliche 1er étage, bureau 1414
34 295 Montpellier Cedex 5
France
National Reference Center of Keratoconus (CRNK), CHU Toulouse, France
Adress
Service d'Ophtalmologie Pavillon Dieulafoy Place du Docteur BaylacTSA 40031
31000 Toulouse
France
Centro Hospitalar e Universitário de Coimbra – CHUC, Coimbra, Portugal
Adress
Praceta Professor Mota Pinto
3004-561 Coimbra
Portugal