Phenotype #0000259300

Individual ID 00363962
Associated disease -
Phenotype details At the age of 28 the fundus of the patient showed numerous yellow-whitish flecks throughout the posterior pole-resorption of the flecks and extensive atrophy of the choriocapillaris in the macula. At that time the Best corrected visual acuity was 0.06 OD and 0.05 OS.
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 18y
Phenotype/Onset visual effects noted for the first time
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2021-05-03 14:25:36 +02:00 (CEST)
Date last edited N/A

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