EURUSH

Clinical Trial

NCT01954953 Unknown

EURUSH

Clinical and Genetic Examination of Usher Syndrome Patients’ Cohort in Europe.

Observational

Disease

Disease type

Hereditary retinal disease

Retinitis Pigmentosa

Usher Syndrome

Orphan drug recognition

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

01/09/2013

Closing date

01/01/2016

Inclusion criteria :

Exclusion criteria :

Funding

public

Members involved

Main investigators

Pr José-Alain Sahel

France

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)

Others investigators

Pr Isabelle Audo

Representative

France

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)