Phenotype #0000262879

Individual ID 00367541
Associated disease -
Phenotype details At the age of 37, the BCVA (RE) was: 20/80 and (LE) was: 20/80. Furthermore, there was: Macular atrophy with yellow?white flecks at the level of the rinal pigment epithelium at the posterior pole reaching the vascular arcades Normal ffERG responses
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 31y
Phenotype/Onset unknown
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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