Phenotype #0000260162

Individual ID 00364824
Associated disease -
Phenotype details Exhibited a central form of cone dysfunction resembling occult macular dystrophy that preceded the development of lipofuscin flecks, atrophy of retinal pigment epithelium (RPE), or full-field electroretinography abnormalities. Final visual acuity was 20/70 (OD) and 20/100 (OS).
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 10y1m
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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