BMJ Case Reports · 2018 · 10 citations · 2 references
MedicineOphthalmologyVision ScienceOcular DiseaseOcular ImagingVisual DisordersMacular DisordersRetinal DisordersRetinal PathologyVisual ImpairmentAutofluorescenceAutofluorescence ImagingFundus Autofluorescence ImagingKearns-sayre SyndromeOphthalmologic ManifestationsOptical Coherence Tomography FindingsPigmentary RetinopathySlit-lamp Examination Findings
An 11-year-old girl with moderate ptosis and chronic progressive ophthalmoplegia (figure 1) was referred for retinal evaluation in view of nyctalopia. Visual acuity on presentation was 20/40 OU. Slit-lamp examination revealed a normal anterior segment. There was no similar family history. Multicolour scanning laser photographs (figure 2A, B) showed retinal pigment granularity in OU that was better appreciated on autofluorescence imaging as speckled hypoautofluorescence and hyperautofluorescence (figure 2C, D). Horizontal spectral domain optical coherence tomography scans …
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