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

NCT00422721 · clinicaltrials.gov ↗

NA

Phase

COMPLETED

Status

360

Enrollment

OTHER

Sponsor class

Conditions

Amaurosis
Retinal 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

Sponsor

Nantes University Hospital