
Dr Elise Boulanger-Scemana
France
HCP Center: Fondation Adolphe de Rothschild, Paris, France
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France
HCP Center: Fondation Adolphe de Rothschild, Paris, France

France
HCP Center: OPHTARA – Hôpital Cochin, Paris, France
Working Group(s): Anterior Segment Rare Eye Diseases (WG4)

Norway
HCP Center: Oslo University Hospital, supporting partner expert’s center
Clinic unit(s): Department of Ophthalmology, Paediatric Ophthalmology, Ophthalmic Genetics & Electrophysiology
Working Group(s): Retinal Rare Eye Diseases (WG1), Pediatric Ophthalmology Rare Diseases (WG3), Genetic Diagnostics (TWG6), Research (TWG8)

Austria
HCP Center: Department of ophthalmology, Kepler University Clinic Linz, Linz, Austria
Working Group(s): Genetic Diagnostics (TWG6)

Representative
France
HCP Center: OPHTARA – AP-HP, Hôpital Necker-Enfants Malades, Paris, France
Working Group Leader: Pediatric Ophthalmology Rare Diseases (WG3)
Other(s) Working Group(s): Retinal Rare Eye Diseases (WG1), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Anterior Segment Rare Eye Diseases (WG4), Low Vision Daily Life and Patients Groups (TWG5), Genetic Diagnostics (TWG6), Registries & Epidemiology (TWG7), Research (TWG8), National Integration (TWG9), CPMS & Digital Medecine (TWG10)

Substitute
Ireland
HCP Center: ERN-EYE Ireland Consortium (EEIC), Dublin, Ireland

Italy
HCP Center: AOU Università degli Studi della Campania Luigi Vanvitelli, Napoli, Italy
Working Group(s): Retinal Rare Eye Diseases (WG1), Genetic Diagnostics (TWG6), Registries & Epidemiology (TWG7)