Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy

NACompletedINTERVENTIONAL
Enrollment

360

Participants

Timeline

Start Date

April 30, 2007

Conditions
AmaurosisRetinal Diseases
Interventions
PROCEDURE

realization of a family tree

PROCEDURE

refractometry

PROCEDURE

evaluation of the presence of a nystagmus

PROCEDURE

ocular behavior

PROCEDURE

test of baby vision

PROCEDURE

test of keenness

PROCEDURE

reading test

PROCEDURE

visual field

PROCEDURE

color vision

PROCEDURE

electroretinographical activity

PROCEDURE

biomicroscopical test

PROCEDURE

retinal imaging

PROCEDURE

retinal autofluorescence

PROCEDURE

genotyping

Trial Locations (1)

44093

CHU de Nantes, Nantes

All Listed Sponsors
lead

Nantes University Hospital

OTHER

NCT00422721 - Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy | Biotech Hunter | Biotech Hunter