Member info
Dr Alejandra Daruich-Matet
France
Working Group(s): Retinal Rare Eye Diseases (WG1), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), National Integration (TWG9)
Team
Pr Dominique BREMOND-GIGNAC
France
Anterior Segment Rare Eye Diseases (WG4), CPMS & Digital Medecine (TWG10), 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
Pr Matthieu Robert
France
Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
HCP Center
The Reference Center for Rare Diseases in Ophthalmology was recognized in 2006
as part of the Rare Diseases Plan 2006-2011, re-labeling in 2017....
contact
OPHTARA – AP-HP, Hôpital Necker-Enfants Malades, Paris, France
Service d'ophtalmologieBât. Lecourbe - RC149 rue de Sèvres
75 015 Paris
France
Scientific publications
CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia
The genotyping analysis identified combined genetic variants of thrombophilia in each patient. Mutations for MTHFR (C677T) and GPIIIa PlA1/A2 were...