Phenotype #0000285082

Individual ID 00391759
Associated disease STGD
Phenotype details Nystagmus - infancy, Photophobia - infancy, visual acuity right/left eye: 20/160: 20/200, Contrast Sensitivity: 0.75:0.60, , Color vision: Strong RG & BY, deficit, Refractive error -11.00/-11.00 × 75, Retinal exam: peripapillary atrophy; dull foveal reflex; peripheral lattice right eye, Fundus autofluorescence: Foveolar hypo AF; parafoveal hyper AF; Optical Coherence Tomography: Mild disruption of outer segments, in central, sub-foveal regio
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite achromatopsia
Age/Examination 19y (19 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-11-18 15:02:57 +01:00 (CET)
Date last edited N/A

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