Phenotype #0000255933

Individual ID 00360528
Associated disease -
Phenotype details Symmetrical disciform areas of retinal pigment epithelial (RPE) atrophy and some interspersed patches ofchoroidal atrophy. However, the foveolar RPE is widely intact. These morphological changes correspond with central visual field defects but only mild foveolar sensitivity losses and normal peripheral fields.
Diagnosis/Initial pseudo-Stargardt disease
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Manon Peeters
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-04-06 16:50:09 +02:00 (CEST)
Date last edited N/A

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