Phenotype #0000260447

Individual ID 00365109
Associated disease -
Phenotype details At the age of 9: Early-onset markedly decreased vision acuity in both eyes along with an increasing difficulty in dark adaptation and a variable loss in color vision. On fundus examination, typical presentations were observed, including some pigment mottling, beaten-bronze macular appearance, and yellow-white flecks around maculae, while few pigmented bone spicules were seen in the retinal periphery. BCVA: 0.15/0.15
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset <10y
Phenotype/Onset decreased visual acuity
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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