Phenotype #0000295817

Individual ID 00403070
Associated disease -
Phenotype details visual acuity right, left eye: 20/25, 20/100; stage, right eye: pseudohypopyon/vitelliruptive_scrambled-egg/cicatricial, left eye: vitelliruptive_scrambled-egg/cicatricial; fluorescein angiography: both eyes: hyperfluorescence, passive leakage into scar; both eyes: mildly increased fundus autofluorescence, left eye: decreased fundus autofluorescence in central part of scar; optical coherence tomography: both eyes: adhesion between retina a underlying hyperreflective cicatricial material, surrounded by hyporeflective subretinal material
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite dystrophy, macular, vitelliform type 2 (VMD2)
Age/Examination 17y (17 years)
Age/Diagnosis -
Age/Onset <5y
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-02-16 14:48:04 +01:00 (CET)
Date last edited N/A

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