Accessibility and reading comfort

Text size

Light/Dark mode

Lines vertical spacing

Trouble using our website?
Contact us

Pr Dominique BREMOND-GIGNAC

In this page

Member info

Pr Dominique BREMOND-GIGNAC

Representative

France

Working Group Leader: Pediatric Ophthalmology Rare Diseases (WG3)
Other 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)

Team

Pr Matthieu Robert

France

Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
See more

Dr Alejandra Daruich-Matet

France

National Integration (TWG9), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
See more

Nathalie De Vergnes

France

Genetic Diagnostics (TWG6)
See more

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

Clinical trials

NCT04561466 Recruiting, Active

Study of the efficacy of Befizal® 200mg in the treatment of Leber’s hereditary optic neuropathy

Interventional
See the trial
voir la fiche
NCT03940690 Suspended

Interest of Intravitreal Injections of Anti-VEGF as Initial and Adjuvant Treatment in Coats Disease.

Interventional
See the trial
voir la fiche

NCT04153344 Completed

Function of the Pigment Epithelium in Patients With Type 1 Neurofibromatosis (NEF-1)

Observational
See the trial
voir la fiche
NCT04125927 Completed

Open-label, Single-arm, Multicenter Study to Assess the Safety of Cystadrops® in Pediatric Cystinosis Patients From 6 Months to Less Than 2 Years Old

Interventional
See the trial
voir la fiche
NCT02771379 Completed

A Non-interventional Study of Clinical Experience in Patients Prescribed Raxone® for the Treatment of Leber’s Hereditary Optic Neuropathy (LHON).

Observational
See the trial
voir la fiche
NCT04276558 Recruiting, Active

Efficacy, Safety and Pharmacokinetics of 3 Doses of REC 0/0559 Eye Drops for the Treatment of Stage 2 (Moderate) and 3 (Severe) Neurotrophic Keratitis in Adult Patients

Interventional
See the trial
voir la fiche
NCT05408715 Recruiting, Active

An International Prospective Natural History Study in Children With a Type II Collagen Disorder With Short Stature

Observational
See the trial
voir la fiche
NCT02970266 Completed

Genetic Decryption of Leber Congenital Amaurosis (LCA) in a Large Cohort of Independent Families.

Observational
See the trial
voir la fiche

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...